Immunologic compositions and methods for studying and treating cancers expressing frizzled antigens

ABSTRACT

This invention is in the field of immunology. More specifically, it relates to compositions and methods for identifying, treating and preventing cancer by targeting the extracellular domains of the frizzled receptor family of proteins.

TECHNICAL FIELD

[0001] This invention is in the field of immunology. More specifically, it relates to compositions and methods for identifying, treating and preventing cancer by targeting the extracellular domains of the frizzled receptor family of proteins.

BACKGROUND OF THE INVENTION

[0002] Many adult cancers arise from small populations of residual tissue stem cells that have a high rate of cell proliferation. These tissue stem cells express various different cell surface receptors and ligands that are used to direct tissue pattern formation and cellular differentiation during development of the embryo, but since these receptors and ligands are not needed in adults, their expression is often very low in differentiated cells. Thus, targeting the immunological differences between the receptors that are expressed by cancers arising from residual tissue stem cells and those found on normal cells may provide for useful cancer therapies.

[0003] In order for cell surface receptors and their associated ligands to be suitable targets for immunotherapies, they should have certain preferred characteristics. First, they should be expressed on the surface of the malignant cells, and to a much lesser degree on normal cells. Second, they should have areas of secondary structures that give rise to conformations which are capable of being recognized by antibodies, cytotoxic T cells and/or drugs. Third, these areas of recognition should be sufficiently different from other cell surface receptors to avoid potentially damaging immunologic cross-reactions.

[0004] The G-protein coupled receptors (GPCRs) are particularly attractive targets for both passive and active immunotherapy, because many of these receptors have all three of these characteristics. In general, they contain seven membrane-spanning regions and a relatively short amino-terminal tail that is exposed into the extracellular environment. This “tail” often assumes a defined secondary structure which is unique to each receptor. In addition to the tail portion, there are other regions in-between the membrane-spanning regions that are also exposed on the cell surface. Accordingly, members of this gene family may be attractive targets for active and passive immunotherapies.

[0005] Frizzled antigens are a family of GPCR-like receptors that have binding sites for Wnt protein ligands, which are secreted molecules that act as upregulators of gene expression via the β-catenin cytoplasmic intermediate pathway. This receptor-ligand pair plays a role in embryonic development, and may play a role in cellular proliferation and the ultimate fate of cells during embryogenesis.

[0006] The presence of frizzled gene products in human cancer cells has previously been suggested. For example, frizzled-2 (FRZ-2) was originally isolated by Sagara et al., who reported that mRNA from frizzled-2 was not detectable in 15 different normal human adult tissues, with the possible exception of heart tissue, but was found in embryonic tissues, as well as six of eight malignant cell lines (Biochem. Biophys. Res. Comm. 252:117-122 (1998)). However, the ultimate expression of the mRNA and the presence of particular frizzled antigens in cancer cells but not in normal cells has not been described.

[0007] There are 18 Wnt and 10 Frizzled genes, all of which are highly homologous in structure, which have been identified thus far from the human genome database (Science, 291:1304-1351 (2001)). However, their high degree of homology and the existence of mRNA encoding these receptors in both normal and tumor tissue would suggest that they would not make a suitable target for immunotherapies.

[0008] Despite their homology and widespread existence, it would be expected that there are certain frizzled proteins that are highly specific for tumors. This is because of their involvement in embryogenesis and the hypothesis that many malignant cells may express embryonic patterning receptors. Accordingly, the present invention relates to the design of immunologic compositions and methods that target the portion of the frizzled antigen that is unique to this protein, specific to cancer cells, and also exposed on the cell surface.

SUMMARY OF THE INVENTION

[0009] The present invention relates, inter alia, to a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein the antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell. In a preferred embodiment, this extracellular domain comprises the amino terminal peptide fragment of the frizzled receptor. The antibody can further comprises an in-tact antibody or a fragment thereof as described in more detail herein. The purified antibody cal also be capable of sensitizing malignant cells expressing the frizzled receptor to a cytotoxic factor. It is also possible that binding of the antibody to the receptor inhibits binding of the Wnt ligand.

[0010] For use in a diagnostic assay, the purified antibody of claim 1 may further comprise a detectable label. In another aspect of the present invention, the antibody may be a human antibody, and may be polyclonal or monoclonal antibody.

[0011] In another embodiment, the present invention relates to an isolated nucleic acid, comprising at least one nucleotide fragment encoding an extracellular domain of a frizzled receptor that serves as an epitope for the antibody just described. In instances when it is necessary to enhance the immunogenicity of the frizzled receptor epitope, one can couple the epitope to a known T cell epitope, such as the tetanus toxin. Accordingly, a frizzled receptor epitope conjugate can be prepared comprising at least one epitope in an extracellular domain of the frizzle receptor expressed on a malignant cell and at least one epitope specific to a T cell antigen. It is also possible to enhance the immunogenicity of any given frizzled receptor epitope by preparing a multimer, such as a dimer or trimer, thereof. Such conjugates can be prepared by direct conjugation, or by making use of a linker moiety, such as the GPSL linker.

[0012] Another aspect of the present invention relates to a transgenic non-human animal which has been transfected with the nucleic acid encoding the frizzled receptor, or a portion thereof. The present invention also relates to a recombinant vector, comprising at least one nucleic acid encoding the frizzled receptor, or a portion thereof, functionally attached to a promoter region upstream of the nucleic acid. In addition, the present invention relates to a host cell comprising at least one such recombinant vector.

[0013] In yet another aspect of the present invention, a pharmaceutical composition is provided which comprises a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein the antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell, in a pharmaceutically acceptable carrier.

[0014] The present invention also relates to a method for modulating a biological activity of a malignant cell that expresses a frizzled receptor comprising administering a pharmaceutical composition comprising a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein the antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell, in a pharmaceutically acceptable carrier.

[0015] In a further embodiment, the present invention relates to a pharmaceutical composition useful as a vaccine against malignancy for administration to a patient having a predisposition for the malignancy, wherein the antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell. Such vaccine can be administered using a method of immunizing a subject against a malignancy comprised of malignant cells that express a frizzled receptor, said method comprising the steps of:

[0016] a) identifying an antibody for modulating a biological activity of the malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell; and

[0017] b) administering the antibody in a pharmaceutically acceptable carrier in an amount sufficient to inhibit the malignancy.

[0018] For use as an immunotherapeutic agent, the present invention relates to a method of treating a subject with a malignancy comprised of malignant cells that express a frizzled receptor, said method comprising the steps of:

[0019] a) identifying an antibody for modulating a biological activity of the malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell; and

[0020] b) administering the antibody in a pharmaceutically acceptable carrier in an amount sufficient to modulate a biological activity of the malignant cell.

[0021] For use as an immunoassay, the present invention relates to an assay for identifying a frizzled receptor expressed by a malignant cell, wherein said frizzled receptor comprises at least one epitope in an extracellular domain, comprising the steps of:

[0022] a) identifying an antibody that specifically binds to the epitope;

[0023] b) exposing a sample of cells suspected of expressing the frizzled receptor to the antibody; and

[0024] c) determining the extent of binding of the antibody to the cells.

[0025] In yet another aspect of the present invention, a screening assay is provided for identification of small molecules that modulate frizzled receptor activity, which comprises:

[0026] a) selecting a library of the small molecules comprising a plurality of different chemical structures;

[0027] b) contacting the small moleucles with an extracellular domain of a frizzled receptor which is capable of binding to its corresponding Wnt protein; and

[0028] c) measuring binding of a ligand to the frizzled receptor in the presence of the small molecule, wherein the ligand is selected from the group consisting of the small molecule, the Wnt protein, and an antibody to the extracellular domain of the frizzled receptor. Such small molecules, which may be nucleic acids, peptides, small organic molecules, or combinations thereof, can function by competing with the Wnt protein for binding to the frizzled receptor, or may mimic the frizzled receptor and bind to the Wnt protein, wherein in the latter instance, the small molecule will prevent binding of both the Wnt protein and an antibody that is specific for the frizzled receptor epitope to which the Wnt protein normally binds from binding thereto. These types of screening methods are well know in the G-protein coupled receptor field, and in particular the field of odorant receptors. See, e.g., U.S. Pat. No. 6,008,000, which discloses assays for screening taste modulating small moleucles that modulate the activity of a G-protein coupled receptor known to be associated with taste.

[0029] Other aspects of the present invention are found throughout the specification.

BRIEF DESCRIPTIONS OF THE DRAWINGS

[0030]FIG. 1 depicts a schematic of the developmental signaling pathways.

[0031]FIG. 2 depicts the alignment of various deduced amino acid sequences of frizzled receptors derived using the Clustal W program on DeCypher. “CY” refers to the cysteine rich domain. “TM” refers to the transmembrane domain. Accordingly, the regions in-between the CRD and TM domains represent the extracellular regions.

[0032]FIG. 3 depicts the sequence alignment of a portion of the first extracellular region of human frizzled receptors.

[0033]FIG. 4 depeits the proliferation of SNU1076 cells as described in Example 3

[0034]FIGS. 5 and 6 depict the effects of anti-Fz Abs on cancer cell apoptosis as described in Example 4.

[0035]FIG. 7 depicts a graphical representation of an olfactory protein, also a G-protein coupled receptor transmembrane protein like the frizzled receptors, showing the amino terminal and three extracellular domain loops, as well as the seven transmembrane domains shown within the cylinders (from PCT WO 92/17585).

[0036]FIG. 8 depicts the sequence alignment of the deduced amino acid sequences of human (HFZ) and mouse (MFZ) frizzled receptors 1 to 10, assigned Seq. ID No.s. 44 to 60 in the order shown. Also depicted therein are the amino terminal domains (assigned Seq. ID No.s 61 to 77 in the order shown), the extracellular domain loop 1 (assigned Seq. ID No.s 78 to 94 in the order shown), the extracellular domain loop 2 (assigned Seq. ID No.s 95 to 111 in the order shown), and the extracellular domain loop 3 (assigned Seq. ID No.s 112 to 128 in the order shown.

DISCLOSURE OF THE INVENTION

[0037] The present invention relates to the use of immunologically unique frizzled receptor epitopes as binding targets in the design of compositions and methods that are useful in immunologic based diagnostics and therapeutics of cancers associated with overexpression of frizzled receptors.

[0038] In embryogenesis, body patterning is related to the axial expression of different proteins. The proximal-distal axis is controlled by fibroblast growth factor (FGF), anterior-posterior axis by Sonic hedgehog (SHH), and the dorsal ventral axis by wingless (Wnt). These factors are closely cross-regulated in development. As shown in FIG. 1, the secretion of Wnt is stimulated by SHH signaling and conversely the expression of SHH is supported by the continued presence of Wnt. SHH in turn influences FGF expression. Wnt has been shown to be a ligand for a G-coupled protein receptor in the frizzled (Fz) family of receptors, which mediates a complex signaling cascade. Transcriptional regulation is also mediated by SHH cell surface interaction with its ligand, Patched. Patched tonically inhibits signaling through Smoothened until it binds to SHH. The Wnt/frizzled pathway has been previously implicated in tumorigenesis. Soluble Wnt glycoproteins have been demonstrated to transmit signal by binding to the seven transmembrane domain G-protein coupled-receptor (FIG. 1). Upon Wnt signaling, a cascade is initiated that results in the accumulation of cytoplasmic beta-catenin and its translocation to the nucleus. In the nucleus beta-catenin binds a specific sequence motif at the N terminus of lymphoid-enhancing factor/T cell factor (LEF/TCF) to generate a transcriptionally active complex. Beta-catenin interacts with multiple other proteins such as cadherin which it links to the cytoskeleton. It also associates with the adenomatous polyposis coli (APC) tumor suppressor protein and glycogen synthetase 3 beta (GSK3β). These proteins function to negatively regulate beta catenin by facilitating phosphorylation near the aminoterminus and thus accelerating its proteolytic degradation.

[0039] The frizzled receptors are a well-characterized family of transmembrane receptor proteins. To date, there are ten known human frizzled proteins that have been identified from the human genome as follows: TABLE I Known Human Frizzled Genes Gene Chromosome Reference FZD1 7a21 Sagara (1988) FZD2 17q21.1 Zhao Z (1995), Sagara (1988) FZD3 8p21 Kirikoshi (2000), Sala 2000 FZD4 11q14-q21 Kirikoshi (1999) FZD5 2q34 Wang Y (1996) FZD6 8q22.3-q23.1 Tokuhara (1998) FZD7 2q33 Sagara (1988) FZD8 10 genome FZD9 7g11.23 Wang, YK (1997) FZD10 12q24.333 Koike, et al. (1999) SMOH 7q31-32 Stone (1996) Xie 1998 FZE3 This gene could be Tanaka, et al. (1998) the same as FZD7

[0040] The alignment of several of these frizzled receptors is shown in FIG. 2. As shown therein, Seq. ID No. 35 is assigned to fz3/mouse; Seq. ID NO. 36 is assigned to fz4/mouse; Seq. ID No. 37 is assigned to fz8/mouse; Seq. ID NO. 38 is assigned to fz5/human; Seq. ID No. 39 is assigned to fzd9/human; Seq. ID No. 40 is assigned to fzdl/rat; Seq. ID No. 41 is assigned to fzd2/rat; Seq. ID No. 42 is assigned to fz/Dros; and Seq. ID No. 43 is assigned to fz/Dros.

[0041] To evaluate frizzled receptors for their potential as tumor-associated antigens, various hematologic and epithelial tumors are screened by amplifying the mRNA in the tumor cells using a known amplification method, such as reverse-transcription-polymerase chain reaction (RT-PCR) using primers that are specific for known frizzled receptor-associated sequences. From the results of this initial screening, subregions of the nucleic acid sequence are identified that encode the extracellular regions of the frizzled receptor and are further amplified. The sequence alignment of a portion of the first extracellular region is shown in FIG. 3. This extracellular amino terminal domain is generally regarded as antigenic, because of its size and ternary structure.

[0042] As mentioned elsewhere herein, the gene sequences of frizzled receptors 1 to 10 are known. Also, as shown in FIG. 8, the sequence alignment of the deduced amino acid sequences of human (HFZ) and mouse (MFZ) frizzled receptors 1 to 10 have been determined, and assigned Seq. ID No.s. 44 to 60 in the order shown. Also depicted therein are the amino terminal domains (assigned Seq. ID No.s 61 to 77 in the order shown), the extracellular domain loop 1 (assigned Seq. ID No.s 78 to 94 in the order shown), the extracellular domain loop 2 (assigned Seq. ID No.s 95 to 111 in the order shown), and the extracellular domain loop 3 (assigned Seq. ID No.s 112 to 128 in the order shown.) For example, Seq. ID No. 95 corresponds to the extracellular domain loop 2 for the HFZ1 receptor shown in FIG. 8c, which is:

[0043] Seq. ID No. 95: GQVDGDVLSGVCFVGLNNVDALRGF

[0044] For convenience, the Seq. ID No. assignments to the human extracellular domains given in FIG. 8 are shown below in Table II: TABLE II Sequence ID No.s of Extracellular Domains of Human Receptors given in FIG. 8 Frizzled # Entire Seq. Amino Terminal Loop 1 Loop 2 Loop 3 1 44 61 78 95 112 2 46 63 80 97 114 3 47 64 81 98 115 4 49 66 83 100 117 5 51 68 85 102 119 6 52 69 86 103 120 7 54 71 88 105 122 8 56 73 90 107 124 9 58 75 92 109 126 10 60 77 94 111 128

[0045] 1. Primers

[0046] A primer is preferably single stranded for maximum efficiency, but may alternatively be in double stranded form. If double stranded, the primer is first treated to separate it from its complementary strand before being used to prepare extension products. Preferably, the primer is a plydeoxyribonucleotide. The primer must be sufficiently long to prime the synthesis of extension products in the presence of the agents for polymerization. The exact lengths of the primers will depend on many factors, including temperature and the source of primer.

[0047] Exemplary primer pairs for known human frizzled genes are shown below in Table II. Table II PCR Primers for Known Human Frizzled Isoforms Forward Primers 5′>3′ Seq. ID 1 Frizzled 1 CCCAGAGCTGCAAGAGCTAC Seq. ID 2 Frizzled 2 GCCGTGCCGCTCTATCTGTGAG Seq. ID 3 Frizzled 3 ATAGGCCTGATCATCTGAATCTCCTTCA Seq. ID 4 Frizzled 4 AACCTCGGCTACAACGTGAGACCAAGAT Seq. ID 5 Frizzled 5 ATCGGCTACAACCTGACGCACA Seq. ID 6 Frizzled 6 TCTGGAATGTTCACCAAACATTGAAACT Seq. ID 7 Frizzled 7 CTCATGAACAAGTTCGGCTTCCAGT Seq. ID 8 Frizzled 8 GATGAGGATGAGAGTGAGGTGACATCC Seq. ID 9 Frizzled 9 CACGCGCTGTGCATGGAG Seq. ID Frizzled 10 CATGGAGGCGCCCAACAAC 10 Reverse Primers 5′>3′ Seq. ID Frizzled 1 CACGATCAGCGTCATAAGGT 11 Seq. ID Frizzled 2 GTGGCGCGGGAAGTGCTC 12 Seq. ID Frizzled 3 TCTTGGCACATCCTCAAGGTAATAGGTT 13 Seq. ID Frizzled 4 GTACTGGATGAGCGGTGTGAAAGTTGT 14 Seq. ID Frizzled 5 ATGGGCGTGTACATAGTGCATAGGAAG 15 Seq. ID Frizzled 6 TTTCTCATAAAGTTTACGACAAGGTGGA 16 Seq. ID Frizzled 7 CGCGGTAGGGTAGGCAGTGG 17 Seq. ID Frizzled 8 ACTCAGACTTCCTGGCTCTCAGGTG 18 Seq. ID Frizzled 9 GGCTCTTCTCCACGTACTGGAACTTCT 19 Seq. ID Frizzled 10 GTCCTTCAGCGGGTGCTCCT 20

[0048] The primers described herein are selected to be “substantially” complementary to the different strands of each specific sequence to be synthesized or amplified. This means that the primer must be sufficiently complementary to hybridize relatively specifically with its intended primer site in the target template strand. Therefore, the primer sequence may or may not reflect the exact sequence of the template. For example, a non-complementary nucleotide fragment can be attached to the 5′ end of the primer, with the remainder of the primer sequence being substantially complementary to the strand. Such non-complementary fragments typically contain an endonuclease restriction site. Alternatively, non-complementary bases or longer sequences can be interspersed into the primer, provided the primer sequence has sufficient complementarity overall with the sequence of the strand to be synthesized or amplified to non-randomly hybridize therewith and thereby form an extension product under polynucleotide synthesizing conditions.

[0049] A frizzled gene-specific primer preferably includes at least about 15 nucleotides, more preferably at least about 20 nucleotides. The primer preferably does not exceed about 30 nucleotides, more preferably about 25 nucleotides, although it can contain fewer nucleotides. Short primer molecules generally require lower temperatures to form sufficiently stable hybrid complexes with the template. Most preferably, the primer includes between about 20 to about 25 nucleotides. The length of the primer will vary inversely with the extent of conservation of the complementary exon sequence. The GC content of the primers should be about 50%.

[0050] Primers can be prepared using a number of methods, including phosphotriester and phosphodiester methods or automated embodiments thereof. The phosphodiester and phosphotriester methods are described in Cruthers, Science, 230:281-285 (1985); Brown et al., Meth. Enzymol., 68:109 (1979); and Nrang et al., Meth. Enzymol., 68:90 (1979). In one automated method, diethylphosphoramidites which can be synthesized as described by Beaucage et al., Tetrahedron letters, 22:1859-1962 (1981) are used as starting materials. A method for synthesizing primer oligonucleotide sequences on a modified solid support is described in U.S. Pat. No. 4,458,066.

[0051] Primer extension reactions are preferably performed using purified DNA from the target organism. Isolation of DNA from cells is routine in the art and there are numerous sources of nucleic acid isolation protocols suited for microorganisms such as bacteria and fungi including mammalian cells (e.g., Sambrook et al., supra, (1989)). Primer extension reactions also can be performed using DNA that has not been purified but is accessible to the primer. The DNA can be accessible naturally in the sample or can be made accessible following one or more processing steps.

[0052] 2. Amplification

[0053] The frizzled gene amplifying primers are used to amplify products from tumor cells in a primer extension reaction. A variety of primer extension reactions can be used with the present methods. Non PCR amplification methods include ligase chain reaction (LCR: Barany et al., PCR Meth. Applic., 1:15-16 (1991)), self-sustained sequence replication (SSR: Muller et al., Histochem. Cell Biol., 108:431-437 (1997)), also known as nucleic acid sequence-based amplification: NASBA) and its new derivative, cooperative amplification of templates by cross-hybridization (CATCH: Ehricht et al., Eur. J Biochem., 243:358-364 (1997)), transcript-based amplification system (AMPLISCRIPT®, Kaylx Biosciences, Nepean, Ontario Canada), replicatable RNA reporter systems based on the Q beta replicase, hybridization-based formats such as strand-displacement amplification (SDA: Becton-Dickinson, Franklin Lakes, N.J.; Walker et al. Nucleic Acids Res., 20:1691-1696 (1992)), and chip-based microarrays such as Affymetrix GeneChip (Fodor et al., Nature, (Lond) 364:555-556 (1993)).

[0054] Signal amplification methods also can be used to enhance detectability such as with the use of compound probes (Fahrlander et al., Bio/Technology, 6:1165-1168 (1988)) or branched probes (Chiron Corp., Emeryville, Calif.; Urdea et al., Nucleic Acids Symp. Ser., 24:197-200 (1991)) as is well known in the art.

[0055] Primer extension by PCR is performed by combining one or more primers with the target nucleic acid and a PCR buffer containing a suitable nucleic acid polymerase. The mixture is thermocycled for a number of cycles, which is typically predetermined, sufficient for the formation of a PCR reaction product, thereby enriching the sample to be assayed for the sequence of interest. Protocols for PCR are well known in the art (e.g., U.S. Pat. Nos. 4,683,192, 4,683,202, 4,800,159, and 4,965,188) and are available from a variety of sources (e.g., PCR Technology: Principles and Applications for DNA Amplification, H. Erlich, ed., Stockton Press, New York (1989); and PCR Protocols: A Guide to Methods and Applications, Innis et al., eds., Academic Press, San Diego, Calif. (1990)).

[0056] PCR is typically carried out by thermocycling, i.e., repeatedly increasing and decreasing the temperature of a PCR reaction admixture within a temperature range whose lower limit is about 30 degrees Celsius (30° C.) to about 55° C., and whose upper limit is about 90° C. to about 100° C. Increasing and decreasing the temperature can be continuous, but is preferably phasic with time periods of relative temperature stability at each of the temperatures favoring polynucleotide synthesis, denaturation and hybridization. Thus, the PCR mixture is heated to about 90-100° C. for about 1 to 10 minutes, preferably from 1 to 4 minutes. After this heating period, the solution is allowed to cool to about 54° C., which is preferable for primer hybridization. The synthesis reaction may occur at room temperature up to a temperature above which the polymerase (inducing agent) no longer functions efficiently. Thus, for example, if Taq DNA polymerase is used as inducing agent, the temperature is generally about 70° C. The thermocycling is repeated until the desired amount of amplified product is produced.

[0057] A single frizzled gene-specific primer pair can be used in each amplification reaction. Alternatively, additional primers from other primers pairs can be included in the reaction. The primers are generally added in molar excess over template DNA. The conditions of the PCR are adjusted depending on a number of factors, including the degree of mismatch, the GC content of the primer, the length of the primer factors affecting PCR conditions, melting temperature of the primer, and product length and placement within the target sequence. Adjustments in the concentrations of the reaction components, especially magnesium concentration, can be used to enhance the conditions for PCR.

[0058] The PCR buffer contains the deoxyribonucleoside triphosphates (i.e., polynucleotide synthesis substrates) dATP, dCTP, dGTP, and dTTP and a polymerase, typically thermostable, all in amounts sufficient for the primer extension (i.e., polynucleotide synthesis) reaction. An exemplary PCR buffer comprises the following: 50 mM KCl; 10 mM Tris-HCl at pH 8.3; 1.5 mM MgCl₂; 0.001% (wt/vol) gelatin, 200 microMolar (μM) dATP, 200 μM dTTP, 200 μM dCTP, 200 μM dGTP, and 2.5 units Thermus aquaticus (Taq) DNA polymerase I (U.S. Pat. No. 4,889,818) per 100 microliters (μL) of buffer.

[0059] The inducing agent may be any compound or system which will function to accomplish the synthesis of primer extension products, including enzymes. Suitable enzymes for this purpose include, for example, E. coli DNA polymerase I, Klenow fragment of E. coli DNA polymerase I, T4 DNA polymerase, other available DNA polymerases, reverse transcriptase, and other enzymes, such as heat-stable enzymes that facilitate combination of the nucleotides in the proper manner to form the primer extension products complementary to each nucleic acid strand. Generally, the synthesis will be initiated at the 3′ end of each primer and proceed in the 5′ direction along the template strand, until synthesis terminates, producing molecules of different lengths. There may be inducing agents, however, which initiate synthesis at the 5′ end and proceed in the above direction, using the same process as described above. Frizzled gene-specific primers suitable for such inducing agents can be designed using the principles elaborated above for inducing agents that extend from the 3′ end.

[0060] The PCR reaction can advantageously be used to incorporate into the product a preselected restriction site useful in later cloning and sequencing of the amplified product. This can be accomplished by synthesizing the primer with the restriction site in the 5′ end of the primer.

[0061] 3. Arrays

[0062] In cases where hybridization assays of multiple tumor cell genomes are desired to be performed simultaneously using the same intronic region-specific probes, it would be convenient to perform such hybridizations in an array format. Such assay formats and minaturizations thereof, i.e. microchip assays, are well known in the literature and could easily be adapted for the assays described herein. For example, see PCT WO 00/03037, which describes screening arrays of nucleotides using specific probes. After compilation of the sequences from a variety of tumor cells, these sequences can be used in a microarray format on a microchip to perform simultaneous hybridization studies with various probes or sequences from other tumor cells.

[0063] Alternatively, such assay formats can be designed for use to study hybridization of an array of frizzled gene-specific sequences with a single tumor cell genome, or an array of the protein products derived from the translation of the frizzled gene sequences of a population of cells, or an array of antibodies to such protein products, or combinations thereof in two-dimensional arrays. Such microarray hybridization assays can easily be performed using a variety of known microchip assay formats and techniques.

[0064] In addition to such arrays, the methods of the present invention can be adapted to an array format to screen small molecule libraries for their ability to modulate the biological activities of metastatic cells. For example, small molecule libraries can be screed as potential ligands for frizzled receptors in an array using the antibodies described herein that bind to the extracellular domains in a competitive (or other) assay format. Small molecules which compete with the antibodies for binding to the frizzled receptor would be candidates for further screening as therapeutic agents, and may include small peptide fragments, nucleic acids or organic compound, or combinations thereof.

[0065] Analysis of nucleic acid from known tumor cells or products produced therefrom by primer extension as described herein also can include analysis of the sequence of the amplified frizzled gene of the tumor cell DNA. For example, amplified products such as from a PCR can be directly cloned by a variety of methods well known in the art (e.g., Ausubel et al., Molecular cloning of PCR products, in: Short Protocols in Molecular Biology, 3rd Ed. John Wiley & Sons, Inc., New York, pp. 15-32 (1997)). Cloning of amplified products can be accomplished using “sticky ends” such as the TA cloning method or by “blunt end” cloning approaches. Alternatively, frizzled gene-specific primers can be designed with endonuclease restriction sites at the 5′ end of the primer which are designed for cutting and insertion into a specified cloning vector. Kits are commercially available for cloning amplified products such as produced in a PCR (e.g., Invitrogen, Inc., San Diego, Calif.).

[0066] Methods for sequencing genes are well known, including the Sanger dideoxy mediated chain-termination approach and the Maxam-Gilbert chemical degradation approach. These and other nucleic acid sequencing methods are described, for example, in Sambrook et al., supra, (1989) (chapter 13). Nucleic acid sequencing can be automated using a number of commercially available instruments.

[0067] Amplified products also can be directly sequenced without cloning the product (e.g., Sambrook et al., supra, (1989) (14.22-14.29)). Amplified products that have been purified, for example, by gel electrophoresis, are suitable for direct sequencing (id.).

[0068] 4. Antibodies

[0069] The present invention relies on the ability to design antigen-antibody binding pairs using the extracellular domains of the frizzled receptor as the antigenic epitope. Such antibodies are useful for detecting tumor-specific frizzled receptor epitopes, as well as for imnimunotherapy of cancers. Although many regions of the extracellular domain may have sufficient size and tertiary structure to be independently antigenic, others may require coupling to T helper epitopes. This can be achieved using techniques that are well known in the art (e.g., Harlow and Lane, “Antibodies: A laboratory Manual,” Cold Spring Harber Laberatory Press (1988)). Although there are numerous T helper epitopes known in the art, tetanus toxin and measles virus fusion (MVF) protein T helper epitopes are exemplary. As used herein, the term “frizzled epitope” refers both to an independently antigenic extracellular domain of a frizzled receptor, as well as one which is coupled to a T helper epitope to enhance immunogenicity.

[0070] An anti-frizzled epitope antibody (“anti-Fz Ab”) is used in its broadest sense to include polyclonal and monoclonal antibodies, as well as polypeptide fragments of antibodies that retain a specific binding affinity for its target antigen of, e.g., at least about 1×10⁵M⁻¹. One skilled in the art would know that antibody fragments such as Fab, F(ab′)₂ and Fv fragments can retain specific binding activity for their target antigen and, thus, are included within the definition of an antibody herein. In addition, the term “antibody” as used herein includes naturally occurring antibodies as well as non-naturally occurring antibodies such as domain-deleted antibodies (Morrison et al., WO 89/07142 ) or single chain Fv (Ladner et al., U.S. Pat. No. 5,250,203). Such non-naturally occurring antibodies can be constructed using solid phase peptide synthesis, can be produced recombinantly or can be obtained, for example, by screening combinatorial libraries consisting of variable heavy chains and variable light chains using known methods, such as those described by Huse et al., Science, 246:1275-1281 (1989).

[0071] Antibodies to frizzled epitopes can be prepared using a substantially purified extracellular region of a frizzled receptor, or a fragment thereof, which can be obtained from natural sources or produced by recombinant DNA methods or chemical synthesis. For example, recombinant DNA methods can be used to express the frizzled gene sequence alone or as a fusion protein, the latter facilitating purification of the antigen and enhancing its immunogenicity.

[0072] Antisera containing polyclonal antibodies reactive with antigenic epitopes of the frizzled receptor can be raised in rabbits, goats or other animals. The resulting antiserum can be processed by purification of an IgG antibody fraction using protein A-Sepharose chromatography and, if desired, can be further purified by affinity chromatography using, for example, Sepharose conjugated with a peptide antigen. The ability of polyclonal antibodies to specifically bind to a given molecule can be manipulated, for example, by dilution or by adsorption to remove crossreacting antibodies to a non-target molecule. Methods to manipulate the specificity of polyclonal antibodies are well known to those in the art (e.g., Harlow and Lane, supra, (1988)).

[0073] A monoclonal antibody specific for the frizzled eptope can be produced using known methods (Harlow and Lane, supra, (1988)). Essentially, spleen cells from a mouse or rat immunized as discussed above are fused to an appropriate myeloma cell line such as SP2/0 myeloma cells to produce hybridoma cells. Cloned hybridoma cell lines can be screened using a labeled frizzled epitope to identify clones that secrete an appropriate monoclonal antibody. A hybridoma that expresses an antibody having a desirable specificity and affinity can be isolated and utilized as a continuous source of monoclonal antibodies. Methods for identifying an anti-Fz Ab having an appropriate specificity and affinity and, therefore, useful in the invention are known in the art and include, for example, enzyme-linked immunoadsorbence assays, radioimmunoassays, precipitin assays and immunohistochemical analyses (e.g., Harlow and Lane, supra, (1988) (chapter 14)).

[0074] An anti-Fz Ab can be characterized by its ability to bind specifically to the cells that express the particular frizzled receptor. In addition, an anti-Fz Ab of the invention can be used to purify frizzled receptors from a biological or experimentally prepared sample. For example, such antibodies can be attached to a solid substrate such as a resin and can be used to affinity purify the frizzled receptor. In addition, the anti-Fz Ab can be used to identify the presence of the frizzled receptor in a sample. In this case, the antibody can be labeled with a detectable label such as a radioisotope, an enzyme, a fluorochrome or biotin. An anti-Fz Ab can be detectably labeled using methods well known in the art (e.g., Harlow and Lane, supra, (1988) (chapter 9)). Following contact of a labeled anti-Fz Ab with a sample, specifically bound labeled antibody can be identified by detecting the label.

[0075] 5. Immunoassays

[0076] The binding of an anti-Fz Ab to the frizzled receptor also can be determined using immunological binding reagents. As used herein, an immunological binding reagent includes any type of biomolecule that is useful to detect an antibody molecule. An immunological binding reagent can include a labeled second antibody. A second antibody generally will be specific for the particular class of the first antibody. For example, if an anti-frizzled epitope antibody (i.e., a first antibody) is of the IgG class, a second antibody will be an anti-IgG antibody. Such second antibodies are readily available from commercial sources. The second antibody can be labeled using a detectable moiety as described above. When a sample is labeled using a second antibody, the sample is first contacted with a first antibody (i.e., anti-Fz Ab), then the sample is contacted with the labeled second antibody, which specifically binds to the first antibody and results in a labeled sample. Alternatively, a labeled second antibody can be one that reacts with a chemical moiety, for example biotin or a hapten that has been conjugated to the first antibody (e.g., Harlow and Lane, supra, (1988) (chapter 9)). Immunological binding agents also can include avidin or streptavidin when the anti-frizzled epitope antibody is labeled with biotin.

[0077] Principally, all conventional immunoassays are suitable for the detection of frizzled receptors. Direct binding as discussed above or competitive tests can be used. In a competitive test, the anti-Fz Ab can be incubated with a sample and with the frizzled receptors or a fragment thereof (produced as described herein) both simultaneously or sequentially. The frizzled receptors from the sample preferably competes with the added frizzled epitope (hapten) of the invention for the binding to the antibody, so that the binding of the antibody to the hapten in accordance with the invention is a measure for the quantity of antigen contained in the sample. In a heterogeneous competitive immunoassay where the liquid phase is separated from the solid phase, both the antibody or the peptide can be labeled or bound to a solid phase. The exact amount of antigen contained in the sample can then be determined in a conventional manner by comparison with a standard treated in the same manner.

[0078] All competitive test formats that are known to the expert can be used for the detection. The detection can be carried out, for example, using the turbidimetric inhibition immunoassay (TINIA) or a latex particle imnmunoassay (LPIA). When a TINIA is used, the peptide or peptide derivative of the invention is bound to a carrier such as dextran (EP-A-0 545 350). This polyhapten competes with the analyte contained in the sample for the binding to the antibody. The formed complex can be determined either turbidimetrically or nephelometrically. When an LPIA is employed, particles, preferably latex particles, are coated with the peptides of the invention and mixed with the antibody of the invention and the sample. When an analyte is present in the sample, agglutination is reduced.

[0079] Enzyme immunoassays (Wisdom, Clin. Chem., 22(8):1243-1255 (1976), and Oellerich, J. Clin. Chem. Clin. Biochem., 18:197-208 (1980)), fluorescence polarization immunoassays (FPIA) (Dandliker et al., J Exp. Med., 122:1029 (1965)), enzyme-multiplied immunoassay technology (EMIT) (Rubenstein, Biochem. Biophys. Res. Comm., 47:846-851 (1972)) or the CEDIA technology (Henderson et al., Clin. Chem., 32:1637-41 (1986)) also are suitable immunological based assays for detection of frizzled receptors.

[0080] 6. Immunotherapeutics

[0081] One aspect of the present invention is the design of immunotherapies for cancer. Wnt signaling through frizzled receptors has been described to inhibit apoptosis. Also, some of the genes that are regulated by TCF/beta-catenin are known to be associated with the cell cycle and cell proliferation. By blocking the binding of Wnt proteins to their receptors via antibodies directed to the extracellular portion of frizzled receptors, this pathway can be interrupted. Thus, it is believed that disruption of the downstream translocation of beta-catenin to the nucleus results in slower tumor growth or death of the cell.

[0082] As used herein, the term “modulating a biological activity of a malignant cell” refers to the ability of the antibody to effect cellular function. These effects may manifest themselves as cell growth inhibition, the ability to elicit a cytotoxic response to the malignant cell, or other such negative effects on the malignancy. Although not wishing to be bound to any particular theory, it is believed that this effect is caused by the antibody binding to the extracellular domain of the frizzled receptor in a way that interferes with the Wnt/frizzled signalling pathway.

[0083] The pharmaceutical compositions of the present invention include therapeutically effective amount of the appropriate anti-Fz Ab in a pharmaceutically acceptable carrier. Such carriers are well known in the art. Examples of appropriate carriers are those that are known for delivery of interferons, such as normal saline, dextrose, etc. The mode of administration of the pharmaceutical composition necessarity depends on the type and location of the target tumor cells. Accordingly, the compositions can be delivered, e.g., parenterally, or typically intraveneously in a solution, suspension or emulsion.

[0084] Pharmaceutical compositions and rouths of administration of aqueous compositions comprise an effective amount of the antibody in the pharmaceutically acceptable carrier. By “pharmaceutically acceptable” it is intended that the compositions do not produce adverse, allergic reactions when administered to the animal or human subject, and such carriers include solvents, dispersion media, coatings and the like. Excipients may also be added, which include, inter alia, antimicrobial agents, isotonicity enhancers, absorption delaying agents, surfactants, dispersants, preservatives, and the like.

[0085] For administration to an animal or human subject, the solutions are necessarily prepared to meet all FDA Office of Biologics standards. As such, they are normally dialozed to remove undesired small molecular weight molecules or lyophilized with other active and excipient ingredients for reconstitution prior to administration. As would be appreciated by one of skill in the art, the administration parameters, such as dosage and timing, will necessarily depend on the type and location of the metastes to be treated and would easily be determined using routine optimization principles based on other like immunotherapeutics. Routes of suitable administration may include injection, intraveneous, intramuscular, subcutaneous, intralesional, and the like. Alternatively, the immunotherapeutics of the present invention can be formulated for other local routes of administration as topicals, inhalants, orthotopic, ophthalmic, and the like.

[0086] An “effective” amount of the immunotherapeutics of the present invention is, of course, determined based on the intended therapeutic goal. As such, a “dosage” of the therapeutic refers to the unit amount of the therapeutic expected to achieve the desired goal, each unit containing a predetermined quantity of the therapeutic to be administered by the appropriate route of administration. Administration may also be spaced out over time to maximize the therapeutic effect, such as two to six administrations spaced out in intervals of several hours to several weeks.

[0087] The course of treatment may be monitoried using appropriate immunoassays. For example, the level of circulating anti-Fz Abs following administration can easily be monitored using labeled anti-immunoglobulin antibodies in any of a number of commercially available assay formats.

EXAMPLES

[0088] The following examples are included for illustrative purposes only and are not intended to limit the scope of the invention.

Example 1 Expression of Frizzled Gene mRNA From Normal and Cancer Cells

[0089] To evaluate frizzled receptors for their potential as tumor associated antigens, the mRNA from various hematologic and epithelial tumors were screened, as well as the MRNA from normal cell lines. In this example total RNA was extracted from HNSCC lines (PCI13, Detroit 562, RPMI 2650, SNU1076, KB, AMC4), a CLL line (Lesch), a Burkitt lymphoma line (Ramos), glioma lines (U87MG, and U373MG), normal human bronchial epithelial cell lines (Clonetics, San Diego, Calif.) and normal oral squamous epithelial (OSE) cells using Trizol® (Gibco, BRL, Grand Island, N.Y.). Reverse transcription was performed using 1□ g of RNA from each sample and the Superscript™ Preamplification kit (Gibco BRL). Different pairs of gene-specific primers based on sequences of cloned human isoforms of the frizzled genes were used for reverse transcriptase-PCR (RT-PCR) analysis.

[0090] The following list summarizes the primer pairs used: FZD2 (Seq. ID 21): 5′-cagcgtcttgcccgaccagatcca-3′ (reverse); (Seq. ID 22) 5′-ctagcgccgctcttcgtgtacctg-3′ (forward). FZD5: (Seq. ID 23) 5′-ttcatgtgcctggtggtgggc-3′ (forward); (Seq. ID 24) 5′-tacacgtgcgacagggacacc-3′ (reverse) G3PDH: (Seq. ID 25) 5′-accacagtccatgccatcac-3′ (forward); (Seq. ID 26) 5′-tacagcaacagggtggtgga-3′ (reverse).

[0091] Frizzled 2 was amplified with 25 cycles of PCR. Frizzled 5 and G3PDH were amplified with 30 cycles of PCR. The amplification products for frizzled 2 and G3PDH are shown. The expression of the frizzled isoforms in cancer cells was confirmed by sequencing.

[0092] In an expanded cell set total RNA was extracted from 14 tumor cell lines, two normal human bronchial epithelial cell lines and 10 normal oral mucosal epithelial cells by using Trizol™. Cancer cell lines consisted of 10 head and neck squamous cell cancers (HNSCC), 2 B-cell tumor cell lines, and 2 glioma cell lines. Two normal human bronchial epithelial cell samples were purchased from Clonetics (San Diego, Calif.). Ten normal oral mucosal cell samples (Oral SC) were obtained from scraping the oral mucosa from 10 volunteers. RT-PCR analysis was performed as described above. These results are shown in Table III below. TABLE III :Summary of frizzled genes detected by RT-PCR in normal and cancer cells Normal (11) Cancer (14) mRNA Oral SC NHBE Glioma HNSCC B cell tumor amlified (10) (2) (2) (10) (2) Frizzled 2 0 1 2 10 2 Frizzled 5 4 1 1 9 1

[0093] As shown, in some instances, the frizzled gene associated mRNA is expressed in overabundance in cancer cells when compared to normal cells.

Example 2 Analysis of Frizzled 2 Protein Expression in Cancer vs. Normal Cells

[0094] To determine the amount of protein expressed in the cells studied in Example 1, adherent cells in culture were harvested and lysed with a solution containing 25 mM Tris HCl, 150 mM KCl, 5 mM EDTA, 1% NP-40, 0.5% sodium deoxycholic acid, 0.1% sodium dodecyl sulfate,1 mM NaVO₃, 1 mM NaF, 20 mM □-glycerophosphate and protease inhibitors. Twenty μg of protein from each cell line was separated by SDS-PAGE and transferred to a PVDF membrane. The membrane was immersed in 2% I-block, 0.05% Tween X in PBS and then incubated with a 1:500 dilution of polyclonal goat anti-human frizzled 2 IgG (Santa Cruz Biotechnology, Santa Cruz, Calif.). These primary antibodies were then detected by horseradish peroxidase-conjugated donkey anti-goat IgG (Santa Cruz) and chemiluminiscence (ECL detection reagents, Amersham Life Science, Aylesbury, UK). To verify relative amount of protein transferred in each lane, the presence of actin was measured with an actin monoclonal antibody (Chemicon International Inc, Temecula, Calif.).

[0095] The result of this experiment (not shown) revealed that, although frizzled 2 associated mRNA was detected by RT-PCR as shown in Table III, no detectable amount of protein was detectable immunologically. These contrasting results indicate that tumor specificity of the frizzled receptors at the protein level cannot accurately be predicted by looking at tumor specificity at the mRNA level.

Example 3 The Effects of Anti-Fz Abs on Cancer Cell Growth

[0096] The ability to block the Wnt-frizzled signaling pathway can provide an effective way of limiting growth of tumor cells. In order to determine the efficacy of using such anti-Fz Abs as an adjunctive passive immunotherapy, such as that observed using humanized anti-HER2 antibodies (Herceptin, Genentech, inc., South San Francisco, Calif.), the effects of anti-frizzled 2 antibodies on the growth of HNSCC cells was studied. Soluble inhibitors of frizzled receptors have ben described to induce apoptosis secondary to their inhibition of frizzled signaling. Accordingly, this experiment was designed to test the efficacy of anti-Fz Abs to perform the same function.

[0097] Cell proliferation was determined by a colorimetric MTT-based assay. Briefly, either 7.5×10³ or 10×10³ SNU1076 cells per well were cultured in a 96 well plate. After 24 hour graded amounts of polyclonal goat anti-human frizzled-2 antibody containing 300 ng, 30 ng, 3 ng, and 0.3 ng were added in the culture medium. The same concentrations of goat serum or Goat antihuman IgG (Fisher Scientific, Pittsburgh, Pa.) were used as an isotype control. On 1, 2, 3, or 4 days after incubating antibody, 20 ul of MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide)-based solution was added to the wells for four hours prior to lysis with 15% SDS, 0.015 M HCl. Absorbances at 570 and 650 nm were measured. The results are depicted in FIG. 4 and also given in Table IV below. Data represent the normalized growth fraction of the specific antibody treated cells to that of the control antibody treated cells (in triplicate). TABLE IV Cell proliferation in presence of anti-Fz Ab FZD 300 ng 30 ng 3 ng 0.3 ng Day 1 87.88 ± 9.04 99.21 ± 9.07 108.68 ± 14.58 112.65 ± 13.50 Day 2 68.50 ± 8.50  86.08 ± 10.80 90.33 ± 6.67 89.18 ± 7.97 Day 3 65.09 ± 9.26 86.03 ± 5.74  75.14 ± 19.08 90.22 ± 2.64 Day 4 53.82 ± 4.20 64.52 ± 7.41  88.19 ± 10.97 81.37 ± 7.07 Day 5 53.75 ± 4.57 81.27 ± 9.04 92.98 ± 8.81 90.84 ± 5.71

[0098] As shown, treatment with antibodies markedly decreases the proliferation of SNU1076 cells. In a control experiment (results not shown), there was not appreciable effect of the same antibody on the growth of normal cells.

Examle 4 The Effects of Anti-Fz Abs on Cancer Cell Apoptosis

[0099] The effects of the anti-Fz Abs from Example 3 on apoptosis of SNU1076 cells was also studied. Cells were grown in RPMI-1640 supplemented with 10% FBS. The cells were treated for 72 hours with 300 ng/ml anti-Fz Ab, or control polyclonal antibodies. Two assays were used to quantify the cytotoxic effect of the antibodies as follows:

[0100] As shown in FIG. 5, cells were detached from the flasks by ftrysin treatment and incubated for 10 minutes in growing medium with 5 μg/ml Propidium iodide and 40 nM DiOC₆ and analyzed by flow cytometry. Viable cells (Alive, right bars) had high DiOC₆ (FL-1) and low PI (FL-3) faiorescence, while apoptotic cells (left bars) had low DiOC₆ (FL-1) and low PI (FL-3) fuiorescence.

[0101] As shown in FIG. 6, cells were detached from the flasks by try-psin treatment and incubated overnight in a hypotonic buffer (0.1% citrate, 0.1% SDS) containing 50 μg/ml PI and 100 μg/ml RNase. The amount of DNA was then measured by flow cytometry, and apoptotic cells were defined as having a DNA content lower than the G₀G₁ levels (sub-G₀ cells).

Example 5 Idenitification of tumor-specific frizzled epitopes

[0102] As described above in Examples 1 to 4, frizzled 2 antigens may be differentially overexpressed in cells of malignant phenotype, whereas many frizzled gene products may be expressed in normal and abnormal cells. Whereas the frizzled 2 systems is exemplary herein, it is readily apparent that tumor specific frizzled antigens from the other frizzled genes are equally attractive targets for cancer immunotherapies. Accordingly, the methods taught herein can easily be adapted to other frizzled genes and their protein products.

[0103] For example, a panel of tumor cells that can be screened are derived from the panel of 60 lines which are being characterized in the NIH Developmental Therapeutics Program. The cell lines that are currently available in the lab include: (non-small cell lung cancer) A549/ATCC, NCI-H226, NCI-H460, HOP-62, HOP-92,(colon cancer) HT29, HCT-116, (breast cancer) MCF7, NCI/ADR-RES, MDA-MB-231/ATCC, T-47D, (ovarian cancer) OVCAR-3, OVCAR-4, SK-OV-3, (leukemia) CCRF-CEM, K-562, MOLT-4, HL-60(TB), RPMI-8226, (renal cell) 786-0, TK-10, (prostate cancer) PC-3, DU-145. Normal control cell lines will be purchased as previously from Clonetics.

[0104] The expression of frizzled proteins can be confirmed with commercially available antibodies to frizzled isoforms, or where none are available, they can easily be prepared using known methods.

[0105] The overall strategy is to use the least conserved region of the frizzled protein, attempting to preserve the most native structure possible and to generate the most potent immune response. The most versatile method for designing vaccines of defined regions is naked plasmid DNA. The advantages are that the vectors can be rapidly redesigned to change the length of sequence that is expressed, discontinuous regions of the protein can be co-expressed, and the DNA sequence of the protein can be fused to other epitopes to enhance antigenicity. It affords the versatility of expressing soluble, membrane bound proteins, or small peptide fragments. Also gene transfer by this technique is a powerful tool to introduce multiple protein elements into the same or separate locations. In this system single or multiple proteins can be locally expressed. Injecting a combination of plasmids expressing antigens and costimulators like B7.1 and B7.2 results in enhanced immune responses.

[0106] Several plasmids have been constructed which are under the control of the cytomegalovirus (CMV) promoter which has been found to enable high levels of antigen expression in injected muscle. The pCMVint vector includes the cytomegalovirus (CMV) E1 promoter, the simian virus (SV40) t-intron, and the SV-40 polyadenylation site. The ACB vector has the same elements except the polyadenylation sequence is from the bovine growth hormone gene. For example, a preferred plasmid construct for frizzled-2 encodes the least homologous region of the frizzled gene between the ninth and tenth cysteine. These cysteines stabilize a configuration that enables antibody binding to the native protein. This polypeptide fragement is fused at the amino terminus or the carboxylterminus via a short linker to a tetanus toxin or measles MvF T helper epitope (see below). These minigenes are constructed with overlapping oligonucleotides. The oligonucleotides are 5′ prime phosphorylated with T4 kinase (Boehringer Mannheim, Indianapolis, Ind.) at room temperature for 30 miniutes, annealed by boiling an equimolar admixture of two complementary oligomers and slow cooling. The double stranded oligonucleotides are then ligated 3′ to the tissue plasminogen leader (TPA) leader into the EcoR47III site in frame and into the BamH1 site of the pBluescript SKII vector. The minigene is then subdloned into the pCMV and pACB vectors between the Pst1 and Xba1 sites as previously described.

[0107] The inserts for the vectors are designed as described above. The frizzled putative B cell epitope is from the published sequence. The tetanus toxin and measles MVF T helper epitopes have been optimized for human codon usage by the most frequently used codon per amino acid. The DNA constructs have an initiating methionine and stop codons added to the 5′ and 3′ ends respectively. The amino acid and DNA sequences are summarized below with the short GPSL linker sequence in bold and the T cell helper epitope underlined. Tetanus toxin epitope fused to a frizzled domain pFZD2-TT Seq. ID 27: MCVGQNHSEDGAPALLTTAPPPGLQPGAGGTPGGPGGGGAPPRYATLEHPFHC -GPSL-VDDALINSTKIYSYFPSV-STOP Seq. ID 28: ATG TGC GTC GGC CAG AAC CAC TCC GAG GAC GGA GCT CCC GCG CTA CTC ACC ACC GCG CCG CCG CCG GGA CTG CAG CCG GGT GCC GGG GGC ACC CCG GGT GGC CCG GGC GGC GGC GGC GCT CCC CCG CGC TAC GCC ACG CTG GAG CAC CCC TTC CAC TGC-GGC CCC AGC CTG-GTG GAC GAC GCC CTG ATC AAC AGC ACC AAG ATC TAC AGC TAC TTT CCC AGC GTG TAG pTT-FZD2 Seq. ID 29: MVDDALINSTKIYSYFPSV-GPSL- CVGQNHSEDGAPALLTTAPPPGLQPGAGGTPGGPGGGGAPPRYATLEHPFHC-STOP Seq. ID 30: ATG GTG GAC GAC GCC CTG ATC AAC AGC ACC AAG ATC TAC AGC TAC TTT CCC AGC GTG-GGC CCC AGC CTG-TGC GTC GGC CAG AAC CAC TCC GAG GAC GGA GCT CCC GCG CTA CTC ACC ACC GCG CCG CCG CCG GGA CTG CAG CCG GGT GCC GGG GGC ACC CCG GGT GGC CCG GGC GGC GGC GGC GCT CCC CCG CGC TAC GCC ACG CTG GAG CAC CCC TTC CAC TGC TAG Measles MVF epitope fused to a frizzled domain PFZD2-MMVF Seq. ID 31: MCVGQNHSEDGAPALLTTAPPPGLQPGAGGTPGGPGGGGAPPRYATLEHPFHC GPSL-KLLSLIKGVIVHRLEGVE-STOP Seq. ID 32: ATG TGC GTC GGC CAG AAC CAC TCC GAG GAC GGA GCT CCC GCG CTA CTC ACC ACC GCG CCG CCG CCG GGA CTG CAG CCG GGT GCC GGG GGC ACC CCG GGT GGC CCG GGC GGC GGC GGC GCT CCC CCG CGC TAC GCC ACG CTG GAG CAC CCC TTC CAC TGC-GGC CCC AGC CTG-AAG CTG CTG AGC CTG ATC AAG GGC GTG ATC GTG CAC CGC CTG GAG GGC GTG GAG TAG PMMVF-FZD2 Seq. ID 33: MKLLSLIKGVIVHRLEGVE-GPSL- CVGQNHSEDGAPALLTTAPPPGLQPGAGGTPGGPGGGGAPPRYATLEHPFHC-STOP Seq. ID 34: ATG AAG CTG CTG AGC CTG ATC AAG GGC GTG ATC GTG CAC CGC CTG GAG GGC GTG GAG-GGC CCC AGC CTG-TGC GTC GGC CAG AAC CAC TCC GAG GAC GGA GCT CCC GCG CTA CTC ACC ACC GCG CCG CCG CCG GGA CTG CAG CCG GGT GCC GGG GGC ACC CCG GGT GGC CCG GGC GGC GGC GGC GCT CCC CCG CGC TAC GCC ACG CTG GAG CAC CCC TTC CAC TGC TAG

[0108] Plasmid DNA is prepared using Qiagen Maxiprep (Chatsworth, Calif.) kits with the modification of adding one tenth volume 10% Triton X-114 (Sigma, St. Louis, Mo.) to the clarified bacterial lysate prior to applying it to a column. Prior to injection the residual endotoxin level is quantified using a limulus extract clot assay (Associates of Cape Cod, Woods Hole, Mass.). A level of ≦5 ng endotoxin/□g DNA need be obtained prior to use in an animal. The DNA is resuspended in a sterile pyrogen free saline solution for injection.

[0109] Twenty-eight female mice are divided into groups of 4 mice each. They are injected in the dermis of the tail with a combination of 50 μg plasmid encoding a costimulator and 50 μg linker plasmid diluted in normal saline at weeks zero, one and two. A group with empty vector is included as a negative control. The groups are as follows: TABLE V Vector groups for expresssion of frizzled-2 receptors Group Plasmid 1 Plasmid 2 A pTT-FZD2 nCMV B pTT-FZD2 nCMVB7-1 C pTT-FZD2 nCMVB7-2 D pFZD2-TT nCMV E pFZD2-TT nCMVB7-1 F pFZD2-TT nCMVB7-2 G — nCMV

[0110] Another group of mice in similar groups is immunized using the pMMVF-FZD2 and pFZD2-MMVF set of linked epitope plasmids. ). The nCMVB7-1 and nCMVB7-2 constructs encode the cDNAs for murine CD80 and CD86 (provided by G. Freeman (Dana-Farber Cancer Institute, Boston, Mass.).

[0111] Mice are bled prior to the start of the experiment and then every two weeks thereafter. Serum is separated and stored at −20° C. prior to testing. On week ten (seven weeks after the last injection) mice are sacrificed. The titers of antibody are tested by anti-peptide ELISA. Ninety-six well plates (Costar)are coated with 50 ul/ well 20 μg/ml peptide in phosphate buffered saline (PBS) overnight at 4° C. The plates are then washed and blocked with 200 ul/ well 2% bovine serum albumin (BSA) in PBS. Sera are diluted in 2% BSA in PBS. After overnight incubation at 4° C. the plates are washed. Bound murine IgG is detected by alkaline phosphatase conjugated-goat anti-murine IgG (Jackson lmmunoresearch Laboratories) followed by p-nitrophenylphosphate substrate. The titration curves for each sera are compared using DeltaSOFT II v. 3.66 (Biometallics, Princeton, N.J.).

[0112] Mice that develop sufficiently high titers of antibody that bind to the peptide are tested for specificity to frizzled 2 by fluorescent cytometry with cells that express the protein by transfection and known tumor cells that have the mRNA. Binding is tested by Western blot analysis of cells that express this isoform and to cells that have been found to express other frizzled family members.

[0113] If the antibody response is weak then the vectors can be redesigned with other known potent T helper epitopes. In addition, other vectors can be designed where the frizzled protein fragment is altered to achieve the most desirable conformation. Another immunization strategy will be to use a prime boost method. The animals are originally injected with plasmid DNA and then are boosted with peptide or recombinant protein in incomplete Freund's adjuvant.

[0114] Once antibodies have been identified that delay cancer cell growth in cell culture, the ability of these antibodies can be tested for potential in vivo efficacy in mice. For example, the H-2^(b) thymoma line EL4 can be used as a syngeneic tumor in C57B1/6 mice. This line is transfected with a human frizzled expression vector and selected in neomycin. The expression vector is made by excising the frizzled containing insert from a pET3a bacterial expression vector with Nde1 and BamH1 and ligating the insert into pcDNA3 which has a CMV promoter and a neomycin selection cassette. Thirty two female C57B1/6 mice are divided into groups of 8 mice each. They are injected in the dermis of the tail with a combination of 50 μg plasmid encoding a costimulator and 50 μg linker plasmid diluted in normal saline at weeks zero, one and two. A group with empty vector is included as a negative control. On day 28 the mice are injected with 20×10⁶ frizzled transfected EL4 cells or untransfected cells. The mice are monitored three times a week for weight, and tumor growth measured with a caliper. Tumor volume is calculated by lengthxwidth²×π/6. Mice are sacrificed four weeks post tumor challenge or if the tumor burden reaches approximately 2000 mm³. Inhibition of tumor growth is determined by ANOVA.

[0115] Polyclonal antibodies may have low levels of cross reactivity with other proteins that are below the detection level of the binding assays but convey a biologic effect. The antibodies may have not only a blocking or a steric effect, but may also be able to cross link the receptor and make it constitutively active. The presence of the effector antibody may be a minor population in the polyclonal sera and the effect may appear insignificant. Whereas a monoclonal would have a pure population and only one effect. However the assay using polyclonal antibodies will determine if the frizzled expressing cell lines are susceptible to anti-proliferative activity in the pool of anti-frizzled IgG. This provides useful information with respect to the methods that are useful for screening panels of monoclonal antibodies.

[0116] The examples set forth above are provided to give those of ordinary skill in the art with a complete disclosure and description of how to make and use the preferred embodiments of the compositions, and are not intended to limit the scope of what the inventors regard as their invention. Modifications of the above-described modes for carrying out the invention that are obvious to persons of skill in the art are intended to be within the scope of the following claims. All publications, patents, and patent applications cited in this specification are incorporated herein by reference as if each such publication, patent or patent application were specifically and individually indicated to be incorporated herein by reference.

1 138 1 20 DNA Artificial Sequence Forward primer 1 cccagagctg caagagctac 20 2 22 DNA Artificial Sequence Forward primer 2 gccgtgccgc tctatctgtg ag 22 3 28 DNA Artificial Sequence Forward primer 3 ataggcctga tcatctgaat ctccttca 28 4 28 DNA Artificial Sequence Forward primer 4 aacctcggct acaacgtgag accaagat 28 5 22 DNA Artificial Sequence Forward primer 5 atcggctaca acctgacgca ca 22 6 28 DNA Artificial Sequence Forward primer 6 tctggaatgt tcaccaaaca ttgaaact 28 7 25 DNA Artificial Sequence Forward primer 7 ctcatgaaca agttcggctt ccagt 25 8 27 DNA Artificial Sequence Forward primer 8 gatgaggatg agagtgaggt gacatcc 27 9 18 DNA Artificial Sequence Forward primer 9 cacgcgctgt gcatggag 18 10 19 DNA Artificial Sequence Forward primer 10 catggaggcg cccaacaac 19 11 20 DNA Artificial Sequence Reverse primer 11 cacgatcagc gtcataaggt 20 12 18 DNA Artificial Sequence Reverse primer 12 gtggcgcggg aagtgctc 18 13 28 DNA Artificial Sequence Reverse primer 13 tcttggcaca tcctcaaggt aataggtt 28 14 27 DNA Artificial Sequence Reverse primer 14 gtactggatg agcggtgtga aagttgt 27 15 27 DNA Artificial Sequence Reverse primer 15 atgggcgtgt acatagtgca taggaag 27 16 28 DNA Artificial Sequence Reverse primer 16 tttctcataa agtttacgac aaggtgga 28 17 20 DNA Artificial Sequence Reverse primer 17 cgcggtaggg taggcagtgg 20 18 25 DNA Artificial Sequence Reverse primer 18 actcagactt cctggctctc aggtg 25 19 27 DNA Artificial Sequence Reverse primer 19 ggctcttctc cacgtactgg aacttct 27 20 20 DNA Artificial Sequence Reverse primer 20 gtccttcagc gggtgctcct 20 21 24 DNA Artificial Sequence FZD2 primer (reverse) 21 cagcgtcttg cccgaccaga tcca 24 22 24 DNA Artificial Sequence FZD2 primer (forward) 22 ctagcgccgc tcttcgtgta cctg 24 23 21 DNA Artificial Sequence FZD 5 primer (forward) 23 ttcatgtgcc tggtggtggg c 21 24 21 DNA Artificial Sequence FZD5 primer (reverse) 24 tacacgtgcg acagggacac c 21 25 20 DNA Artificial Sequence G3PDH primer (forward) 25 accacagtcc atgccatcac 20 26 20 DNA Artificial Sequence G3PDH primer (reverse) 26 tacagcaaca gggtggtgga 20 27 75 PRT Artificial Sequence pFZD2-TT 27 Met Cys Val Gly Gln Asn His Ser Glu Asp Gly Ala Pro Ala Leu Leu 1 5 10 15 Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro Gly Ala Gly Gly Thr Pro 20 25 30 Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro Arg Tyr Ala Thr Leu Glu 35 40 45 His Pro Phe His Cys Gly Pro Ser Leu Val Asp Asp Ala Leu Ile Asn 50 55 60 Ser Thr Lys Ile Tyr Ser Tyr Phe Pro Ser Val 65 70 75 28 228 DNA Artificial Sequence Coding region for pFZD2-TT 28 atgtgcgtcg gccagaacca ctccgaggac ggagctcccg cgctactcac caccgcgccg 60 ccgccgggac tgcagccggg tgccgggggc accccgggtg gcccgggcgg cggcggcgct 120 cccccgcgct acgccacgct ggagcacccc ttccactgcg gccccagcct ggtggacgac 180 gccctgatca acagcaccaa gatctacagc tactttccca gcgtgtag 228 29 75 PRT Artificial Sequence pTT-FZD2 29 Met Val Asp Asp Ala Leu Ile Asn Ser Thr Lys Ile Tyr Ser Tyr Phe 1 5 10 15 Pro Ser Val Gly Pro Ser Leu Cys Val Gly Gln Asn His Ser Glu Asp 20 25 30 Gly Ala Pro Ala Leu Leu Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro 35 40 45 Gly Ala Gly Gly Thr Pro Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro 50 55 60 Arg Tyr Ala Thr Leu Glu His Pro Phe His Cys 65 70 75 30 228 DNA Artificial Sequence Coding region for pTT-FZD2 30 atggtggacg acgccctgat caacagcacc aagatctaca gctactttcc cagcgtgggc 60 cccagcctgt gcgtcggcca gaaccactcc gaggacggag ctcccgcgct actcaccacc 120 gcgccgccgc cgggactgca gccgggtgcc gggggcaccc cgggtggccc gggcggcggc 180 ggcgctcccc cgcgctacgc cacgctggag caccccttcc actgctag 228 31 75 PRT Artificial sequence PFZD2-MMVF 31 Met Cys Val Gly Gln Asn His Ser Glu Asp Gly Ala Pro Ala Leu Leu 1 5 10 15 Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro Gly Ala Gly Gly Thr Pro 20 25 30 Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro Arg Tyr Ala Thr Leu Glu 35 40 45 His Pro Phe His Cys Gly Pro Ser Leu Lys Leu Leu Ser Leu Ile Lys 50 55 60 Gly Val Ile Val His Arg Leu Glu Gly Val Glu 65 70 75 32 228 DNA Artificial Sequence Coding region for PFZD2-MMVF 32 atgtgcgtcg gccagaacca ctccgaggac ggagctcccg cgctactcac caccgcgccg 60 ccgccgggac tgcagccggg tgccgggggc accccgggtg gcccgggcgg cggcggcgct 120 cccccgcgct acgccacgct ggagcacccc ttccactgcg gccccagcct gaagctgctg 180 agcctgatca agggcgtgat cgtgcaccgc ctggagggcg tggagtag 228 33 75 PRT Artificial Sequence PMMVF-FZD2 33 Met Lys Leu Leu Ser Leu Ile Lys Gly Val Ile Val His Arg Leu Glu 1 5 10 15 Gly Val Glu Gly Pro Ser Leu Cys Val Gly Gln Asn His Ser Glu Asp 20 25 30 Gly Ala Pro Ala Leu Leu Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro 35 40 45 Gly Ala Gly Gly Thr Pro Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro 50 55 60 Arg Tyr Ala Thr Leu Glu His Pro Phe His Cys 65 70 75 34 228 DNA Artificial Sequence Coding region for PMMVF-FZD2 34 atgaagctgc tgagcctgat caagggcgtg atcgtgcacc gcctggaggg cgtggagggc 60 cccagcctgt gcgtcggcca gaaccactcc gaggacggag ctcccgcgct actcaccacc 120 gcgccgccgc cgggactgca gccgggtgcc gggggcaccc cgggtggccc gggcggcggc 180 ggcgctcccc cgcgctacgc cacgctggag caccccttcc actgctag 228 35 517 PRT Mouse 35 Met Ala Val Ser Trp Ile Val Phe Asp Leu Trp Leu Leu Thr Val Phe 1 5 10 15 Leu Gly Gln Ile Gly Gly His Ser Leu Phe Ser Cys Glu Pro Ile Thr 20 25 30 Leu Arg Met Cys Gln Asp Leu Pro Tyr Asn Thr Thr Phe Met Pro Asn 35 40 45 Leu Leu Asn His Tyr Asp Gln Gln Thr Ala Ala Leu Ala Met Glu Pro 50 55 60 Phe His Pro Met Val Asn Leu Asp Cys Ser Arg Asp Phe Arg Pro Phe 65 70 75 80 Leu Cys Ala Leu Tyr Ala Pro Ile Cys Met Glu Tyr Gly Arg Val Thr 85 90 95 Leu Pro Cys Arg Arg Leu Cys Gln Arg Ala Tyr Ser Glu Cys Ser Lys 100 105 110 Leu Met Glu Met Phe Gly Val Pro Trp Pro Glu Asp Met Glu Cys Ser 115 120 125 Arg Phe Pro Asp Cys Asp Glu Pro Tyr Pro Arg Leu Val Asp Leu Asn 130 135 140 Leu Val Gly Asp Pro Thr Glu Tyr Ser Phe Leu His Val Arg Asp Cys 145 150 155 160 Ser Pro Pro Cys Pro Asn Met Tyr Phe Arg Arg Glu Glu Leu Ser Phe 165 170 175 Ala Arg Tyr Phe Ile Gly Leu Ile Ser Ile Ile Cys Leu Ser Ala Thr 180 185 190 Leu Phe Thr Phe Leu Thr Phe Leu Ile Asp Val Thr Arg Phe Arg Tyr 195 200 205 Pro Glu Arg Pro Ile Ile Phe Tyr Ala Val Cys Tyr Met Met Val Ser 210 215 220 Leu Ile Phe Phe Ile Gly Phe Leu Leu Glu Asp Arg Val Ala Cys Asn 225 230 235 240 Ala Ser Ser Pro Ala Gln Tyr Lys Ala Ser Thr Val Thr Gln Gly Ser 245 250 255 His Asn Lys Ala Cys Thr Met Leu Phe Met Val Leu Tyr Phe Phe Thr 260 265 270 Met Ala Gly Ser Val Trp Trp Val Ile Leu Thr Ile Thr Trp Phe Leu 275 280 285 Ala Ala Val Pro Lys Trp Gly Ser Glu Ala Ile Glu Lys Lys Ala Leu 290 295 300 Leu Phe His Ala Ser Ala Trp Gly Ile Pro Gly Thr Leu Thr Ile Ile 305 310 315 320 Leu Leu Ala Met Asn Lys Ile Glu Gly Asp Asn Ile Ser Gly Val Cys 325 330 335 Phe Val Gly Leu Tyr Asp Val Asp Ala Leu Arg Tyr Phe Val Leu Ala 340 345 350 Pro Leu Cys Leu Tyr Val Val Val Gly Val Ser Leu Leu Leu Ala Gly 355 360 365 Ile Ile Ser Leu Asn Arg Val Arg Ile Glu Ile Pro Leu Glu Lys Glu 370 375 380 Asn Gln Asp Lys Leu Val Lys Phe Met Ile Arg Ile Gly Val Phe Ser 385 390 395 400 Ile Leu Tyr Leu Val Pro Leu Leu Val Val Ile Gly Cys Tyr Phe Tyr 405 410 415 Glu Gln Ala Tyr Arg Gly Ile Trp Glu Thr Thr Trp Ile Gln Glu Arg 420 425 430 Cys Arg Glu Tyr His Ile Pro Cys Pro Tyr Gln Val Thr Gln Met Ser 435 440 445 Arg Pro Asp Leu Ile Leu Phe Leu Met Lys Tyr Leu Met Ala Leu Ile 450 455 460 Val Gly Ile Pro Ser Ile Phe Trp Val Gly Ser Lys Lys Thr Cys Phe 465 470 475 480 Glu Trp Ala Ser Phe Phe His Gly Arg Arg Lys Lys Glu Ile Val Asn 485 490 495 Glu Ser Arg Gln Val Leu Gln Glu Pro Asp Phe Ala Gln Ser Leu Leu 500 505 510 Arg Asp Pro Asn Thr 515 36 500 PRT Mouse 36 Met Ala Trp Pro Gly Thr Gly Pro Ser Ser Arg Gly Ala Pro Gly Gly 1 5 10 15 Val Gly Leu Arg Leu Gly Leu Leu Leu Gln Phe Leu Leu Leu Leu Arg 20 25 30 Pro Thr Leu Gly Phe Gly Asp Glu Glu Glu Arg Arg Cys Asp Pro Ile 35 40 45 Arg Ile Ala Met Cys Gln Asn Leu Gly Tyr Asn Val Thr Lys Met Pro 50 55 60 Asn Leu Val Gly His Glu Leu Gln Thr Asp Ala Glu Leu Gln Leu Thr 65 70 75 80 Thr Phe Thr Pro Leu Ile Gln Tyr Gly Cys Ser Ser Gln Leu Gln Phe 85 90 95 Phe Leu Cys Ser Val Tyr Val Pro Met Cys Thr Glu Lys Ile Asn Ile 100 105 110 Pro Ile Gly Pro Cys Gly Gly Met Cys Leu Ser Val Lys Arg Arg Cys 115 120 125 Glu Pro Val Leu Arg Glu Phe Gly Phe Ala Trp Pro Asp Thr Leu Asn 130 135 140 Cys Ser Lys Phe Pro Pro Gln Asn Asp His Asn His Met Cys Met Glu 145 150 155 160 Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr Pro Leu Asn 165 170 175 Cys Val Leu Lys Cys Gly Tyr Asp Ala Gly Leu Tyr Ser Arg Ser Ala 180 185 190 Lys Glu Phe Thr Asp Ile Trp Met Ala Val Trp Ala Ser Leu Cys Phe 195 200 205 Ile Ser Thr Thr Phe Thr Val Leu Thr Phe Leu Ile Asp Ser Ser Arg 210 215 220 Phe Ser Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Met Cys Tyr Asn 225 230 235 240 Ile Tyr Ser Ile Ala Tyr Ile Val Arg Leu Thr Val Gly Arg Glu Arg 245 250 255 Ile Ser Cys Asp Phe Glu Glu Ala Ala Glu Pro Val Leu Ile Gln Glu 260 265 270 Gly Leu Lys Asn Thr Gly Cys Ala Ile Ile Phe Leu Leu Met Tyr Phe 275 280 285 Phe Gly Met Ala Ser Ser Ile Trp Trp Val Ile Leu Thr Leu Thr Trp 290 295 300 Phe Leu Ala Ala Gly Leu Lys Trp Gly His Glu Ala Ile Glu Met His 305 310 315 320 Ser Ser Tyr Phe His Ile Ala Ala Trp Ala Ile Pro Ala Val Lys Thr 325 330 335 Ile Val Ile Leu Ile Met Arg Leu Val Asp Ala Asp Glu Leu Thr Gly 340 345 350 Leu Cys Tyr Val Gly Asn Gln Asn Leu Asp Ala Leu Thr Gly Phe Val 355 360 365 Val Ala Pro Leu Phe Thr Tyr Leu Val Ile Gly Thr Leu Phe Ile Ala 370 375 380 Ala Gly Leu Val Ala Leu Phe Lys Ile Arg Ser Asn Leu Gln Lys Asp 385 390 395 400 Gly Thr Lys Thr Asp Lys Leu Glu Arg Leu Met Val Lys Ile Gly Val 405 410 415 Phe Ser Val Leu Tyr Thr Val Pro Ala Thr Cys Val Ile Ala Cys Tyr 420 425 430 Phe Tyr Glu Ile Ser Asn Trp Ala Leu Phe Arg Tyr Ser Ala Asp Asp 435 440 445 Ser Asn Met Ala Val Glu Met Leu Lys Ile Phe Met Ser Leu Leu Val 450 455 460 Gly Ile Thr Ser Gly Met Trp Ile Trp Ser Ala Lys Thr Leu His Thr 465 470 475 480 Trp Gln Lys Cys Ser Asn Arg Leu Val Asn Ser Gly Lys Val Lys Arg 485 490 495 Glu Lys Arg Gly 500 37 599 PRT Mouse 37 Met Glu Trp Gly Tyr Leu Leu Glu Val Thr Ser Leu Leu Ala Ala Leu 1 5 10 15 Ala Val Leu Gln Arg Ser Ser Gly Ala Ala Ala Ala Ser Ala Lys Glu 20 25 30 Leu Ala Cys Gln Glu Ile Thr Val Pro Leu Cys Lys Gly Ile Gly Tyr 35 40 45 Asn Tyr Thr Tyr Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu 50 55 60 Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys 65 70 75 80 Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro Ile Cys 85 90 95 Leu Glu Asp Tyr Lys Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu 100 105 110 Arg Ala Lys Ala Gly Cys Ala Pro Leu Met Arg Gln Tyr Gly Phe Ala 115 120 125 Trp Pro Asp Arg Met Arg Cys Asp Arg Leu Pro Glu Gln Gly Asn Pro 130 135 140 Asp Thr Leu Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala 145 150 155 160 Pro Ser Pro Pro Arg Arg Leu Pro Pro Pro Pro Pro Pro Gly Glu Gln 165 170 175 Pro Pro Ser Gly Ser Gly His Ser Arg Pro Pro Gly Ala Arg Pro Pro 180 185 190 His Arg Gly Gly Ser Ser Arg Gly Ser Gly Asp Ala Ala Ala Ala Pro 195 200 205 Pro Ser Arg Gly Gly Lys Thr Gly Gln Ile Ala Asn Cys Ala Leu Pro 210 215 220 Cys His Asn Pro Phe Phe Ser Gln Asp Glu Arg Ala Phe Thr Val Phe 225 230 235 240 Trp Ile Gly Leu Trp Ser Val Leu Cys Phe Val Ser Thr Phe Ala Thr 245 250 255 Val Ser Thr Phe Leu Ile Asp Met Glu Arg Phe Lys Tyr Pro Glu Arg 260 265 270 Pro Ile Ile Phe Leu Ser Ala Cys Tyr Leu Phe Val Ser Val Gly Tyr 275 280 285 Leu Val Arg Leu Val Ala Gly His Glu Lys Val Ala Cys Ser Gly Gly 290 295 300 Ala Pro Gly Ala Gly Gly Arg Gly Gly Ala Gly Gly Ala Ala Ala Ala 305 310 315 320 Gly Ala Gly Ala Ala Gly Arg Gly Ala Ser Ser Pro Gly Ala Arg Gly 325 330 335 Glu Tyr Glu Glu Leu Gly Ala Val Glu Gln His Val Arg Tyr Glu Thr 340 345 350 Thr Gly Pro Ala Leu Cys Thr Val Val Phe Leu Leu Val Tyr Phe Phe 355 360 365 Gly Met Ala Ser Ser Ile Trp Trp Val Ile Leu Ser Leu Thr Trp Phe 370 375 380 Leu Ala Ala Gly Met Lys Trp Gly Asn Glu Ala Ile Ala Gly Tyr Ser 385 390 395 400 Gln Tyr Phe His Leu Ala Ala Trp Leu Val Pro Ser Val Lys Ser Ile 405 410 415 Ala Val Leu Ala Leu Ser Ser Val Asp Gly Asp Pro Val Ala Gly Ile 420 425 430 Cys Tyr Val Gly Asn Gln Ser Leu Asp Asn Leu Arg Gly Phe Val Leu 435 440 445 Ala Pro Leu Val Ile Tyr Leu Phe Ile Gly Thr Met Phe Leu Leu Ala 450 455 460 Gly Phe Val Ser Leu Phe Arg Ile Arg Ser Val Ile Lys Gln Gln Gly 465 470 475 480 Gly Pro Thr Lys Thr His Lys Leu Glu Lys Leu Met Ile Arg Leu Gly 485 490 495 Leu Phe Thr Val Leu Tyr Thr Val Pro Ala Ala Val Val Val Ala Cys 500 505 510 Leu Phe Tyr Glu Gln His Asn Arg Pro Arg Trp Glu Ala Thr His Asn 515 520 525 Cys Pro Cys Leu Arg Asp Leu Gln Pro Asp Gln Ala Arg Arg Pro Asp 530 535 540 Tyr Ala Val Phe Met Leu Lys Tyr Phe Met Cys Leu Val Val Gly Ile 545 550 555 560 Thr Ser Gly Val Trp Val Trp Ser Gly Lys Thr Leu Glu Ser Trp Arg 565 570 575 Ala Leu Cys Thr Arg Cys Cys Trp Ala Ser Lys Gly Ala Ala Val Gly 580 585 590 Ala Gly Ala Gly Gly Ser Gly 595 38 516 PRT Homo sapiens 38 Met Ala Arg Pro Asp Pro Ser Ala Pro Pro Ser Leu Leu Leu Leu Leu 1 5 10 15 Leu Ala Gln Leu Val Gly Arg Ala Ala Ala Ala Ser Lys Ala Pro Val 20 25 30 Cys Gln Glu Ile Thr Val Pro Met Cys Arg Gly Ile Gly Tyr Asn Leu 35 40 45 Thr His Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu Ala Gly 50 55 60 Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys Ser Pro 65 70 75 80 Asp Leu Arg Phe Phe Leu Cys Thr Met Tyr Thr Pro Ile Cys Leu Pro 85 90 95 Asp Tyr His Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu Arg Ala 100 105 110 Lys Ala Gly Cys Ser Pro Leu Met Arg Gln Tyr Gly Phe Ala Trp Pro 115 120 125 Glu Arg Met Ser Cys Asp Arg Leu Pro Val Leu Gly Arg Asp Ala Glu 130 135 140 Val Leu Cys Met Asp Tyr Asn Arg Ser Glu Ala Thr Thr Ala Pro Pro 145 150 155 160 Arg Pro Phe Pro Ala Lys Pro Thr Leu Pro Gly Pro Pro Gly Ala Pro 165 170 175 Ala Ser Gly Gly Arg Thr Gly Gln Val Pro Asn Cys Ala Val Pro Cys 180 185 190 Tyr Gln Pro Ser Phe Ser Ala Asp Glu Arg Thr Phe Ala Thr Phe Trp 195 200 205 Ile Gly Leu Trp Ser Val Leu Cys Phe Ile Ser Thr Ser Thr Thr Val 210 215 220 Ala Thr Phe Leu Ile Asp Met Asp Thr Phe Arg Tyr Pro Glu Arg Pro 225 230 235 240 Ile Ile Phe Leu Ser Ala Cys Tyr Leu Cys Val Ser Leu Gly Phe Leu 245 250 255 Val Arg Leu Val Val Gly His Ala Ser Val Ala Cys Ser Arg Glu His 260 265 270 Asn His Ile His Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr Ile Val 275 280 285 Phe Leu Leu Val Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp Val 290 295 300 Ile Leu Ser Leu Thr Trp Phe Leu Ala Ala Ala Met Lys Trp Gly Asn 305 310 315 320 Glu Ala Ile Ala Gly Tyr Gly Gln Tyr Phe His Leu Ala Ala Trp Leu 325 330 335 Ile Pro Ser Val Lys Ser Ile Thr Ala Leu Ala Leu Ser Ser Val Asp 340 345 350 Gly Asp Pro Val Ala Gly Ile Cys Tyr Val Gly Asn Gln Asn Leu Asn 355 360 365 Ser Leu Arg Arg Phe Val Leu Gly Pro Leu Val Leu Tyr Leu Leu Val 370 375 380 Gly Thr Leu Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg 385 390 395 400 Ser Val Ile Lys Gln Gly Gly Thr Lys Thr Asp Lys Leu Glu Lys Leu 405 410 415 Met Ile Arg Ile Gly Ile Phe Thr Leu Leu Tyr Thr Val Pro Ala Ser 420 425 430 Ile Val Val Ala Cys Tyr Leu Tyr Glu Gln His Tyr Arg Glu Ser Trp 435 440 445 Glu Ala Ala Leu Thr Cys Ala Cys Pro Gly His Asp Thr Gly Gln Pro 450 455 460 Arg Ala Lys Pro Glu Tyr Trp Val Leu Met Leu Lys Tyr Phe Met Cys 465 470 475 480 Leu Val Val Gly Ile Thr Ser Gly Val Trp Ile Trp Ser Gly Lys Thr 485 490 495 Val Glu Ser Trp Arg Arg Phe Thr Ser Arg Cys Cys Cys Arg Pro Arg 500 505 510 Arg Gly His Lys 515 39 533 PRT Homo sapiens 39 Met Ala Val Ala Pro Leu Arg Gly Ala Leu Leu Leu Trp Gln Leu Leu 1 5 10 15 Ala Ala Gly Gly Ala Ala Leu Glu Ile Gly Arg Phe Asp Pro Glu Arg 20 25 30 Gly Arg Gly Ala Ala Pro Cys Gln Ala Val Glu Ile Pro Met Cys Arg 35 40 45 Gly Ile Gly Tyr Asn Leu Thr Arg Met Pro Asn Leu Leu Gly His Thr 50 55 60 Ser Gln Gly Glu Ala Ala Ala Glu Leu Ala Glu Phe Ala Pro Leu Val 65 70 75 80 Gln Tyr Gly Cys His Ser His Leu Arg Phe Phe Leu Cys Ser Leu Tyr 85 90 95 Ala Pro Met Cys Thr Asp Gln Val Ser Thr Pro Ile Pro Ala Cys Arg 100 105 110 Pro Met Cys Glu Gln Ala Arg Leu Arg Cys Ala Pro Ile Met Glu Gln 115 120 125 Phe Asn Phe Gly Trp Pro Asp Ser Leu Asp Cys Ala Arg Leu Pro Thr 130 135 140 Arg Asn Asp Pro His Ala Leu Cys Met Glu Ala Pro Glu Asn Ala Thr 145 150 155 160 Ala Gly Pro Ala Glu Pro His Lys Gly Leu Gly Met Leu Pro Val Ala 165 170 175 Pro Arg Pro Ala Arg Pro Pro Gly Arg Ser Cys Ala Pro Arg Cys Gly 180 185 190 Pro Gly Val Glu Val Phe Trp Ser Arg Arg Asp Lys Asp Phe Ala Leu 195 200 205 Val Trp Met Ala Val Trp Ser Ala Leu Cys Phe Phe Ser Thr Ala Phe 210 215 220 Thr Val Leu Thr Phe Leu Leu Glu Pro His Arg Phe Gln Tyr Pro Glu 225 230 235 240 Arg Pro Ile Ile Phe Leu Ser Met Cys Tyr Asn Val Tyr Ser Leu Ala 245 250 255 Phe Leu Ile Arg Ala Val Ala Gly Ala Gln Ser Val Ala Cys Asp Gln 260 265 270 Glu Ala Gly Ala Leu Tyr Val Ile Gln Glu Gly Leu Glu Asn Thr Gly 275 280 285 Cys Thr Leu Val Phe Leu Leu Leu Tyr Tyr Phe Gly Met Ala Ser Ser 290 295 300 Leu Trp Trp Val Val Leu Thr Leu Thr Trp Phe Leu Ala Ala Gly Lys 305 310 315 320 Lys Trp Gly His Glu Ala Ile Glu Ala His Gly Ser Tyr Phe His Met 325 330 335 Ala Ala Trp Gly Leu Pro Ala Leu Lys Thr Ile Val Ile Leu Thr Leu 340 345 350 Arg Lys Val Ala Gly Asp Glu Leu Thr Gly Leu Cys Tyr Val Ala Ser 355 360 365 Thr Asp Ala Ala Ala Leu Thr Gly Phe Val Leu Val Pro Leu Ser Gly 370 375 380 Tyr Leu Val Leu Gly Ser Ser Phe Leu Leu Thr Gly Phe Val Ala Leu 385 390 395 400 Phe His Ile Arg Lys Ile Met Lys Thr Gly Gly Thr Asn Thr Glu Lys 405 410 415 Leu Glu Lys Leu Met Val Lys Ile Gly Val Phe Ser Ile Leu Tyr Thr 420 425 430 Val Pro Ala Thr Cys Val Ile Val Cys Tyr Val Tyr Glu Arg Leu Asn 435 440 445 Met Asp Phe Trp Arg Leu Arg Ala Thr Glu Gln Pro Cys Ala Ala Ala 450 455 460 Ala Gly Pro Gly Gly Arg Arg Asp Cys Ser Leu Pro Gly Gly Ser Val 465 470 475 480 Pro Thr Val Ala Val Phe Met Leu Lys Ile Phe Met Ser Leu Val Val 485 490 495 Gly Ile Thr Ser Gly Val Trp Val Trp Ser Ser Lys Thr Phe Gln Thr 500 505 510 Trp Gln Ser Leu Cys Tyr Arg Lys Ile Ala Ala Gly Arg Ala Arg Ala 515 520 525 Lys Ala Cys Arg Ala 530 40 544 PRT Rat 40 Leu Glu Ala Pro Leu Leu Leu Gly Val Arg Ala Gln Pro Ala Gly Gln 1 5 10 15 Val Ser Gly Pro Gly Gln Gln Arg Pro Pro Pro Pro Gln Pro Gln Gln 20 25 30 Gly Gly Gln Gln Tyr Asn Gly Glu Arg Gly Ile Ser Ile Pro Asp His 35 40 45 Gly Tyr Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala Tyr 50 55 60 Asn Gln Thr Ile Met Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp 65 70 75 80 Ala Gly Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys 85 90 95 Ser Ala Glu Leu Lys Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys 100 105 110 Thr Val Leu Glu Gln Ala Leu Pro Pro Cys Arg Ser Leu Cys Glu Arg 115 120 125 Ala Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro 130 135 140 Asp Thr Leu Lys Cys Glu Lys Phe Pro Val His Gly Ala Gly Glu Leu 145 150 155 160 Cys Val Gly Gln Asn Thr Ser Asp Lys Gly Thr Pro Thr Pro Ser Leu 165 170 175 Leu Pro Glu Phe Trp Thr Ser Asn Pro Gln His Gly Leu Gly Glu Lys 180 185 190 Asp Cys Gly Ala Pro Cys Glu Pro Thr Lys Val Tyr Gly Leu Met Tyr 195 200 205 Phe Gly Pro Glu Glu Leu Arg Phe Ser Arg Thr Trp Ile Gly Ile Trp 210 215 220 Ser Val Leu Cys Cys Ala Ser Thr Leu Phe Thr Val Leu Thr Tyr Leu 225 230 235 240 Val Asp Met Arg Arg Phe Ser Tyr Pro Glu Arg Pro Ile Ile Phe Leu 245 250 255 Ser Gly Cys Tyr Thr Ala Val Ala Val Ala Tyr Ile Ala Gly Phe Leu 260 265 270 Leu Glu Asp Arg Val Val Cys Asn Asp Lys Phe Ala Glu Asp Gly Ala 275 280 285 Arg Thr Val Ala Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu Phe 290 295 300 Met Met Leu Tyr Phe Phe Ser Met Ala Ser Ser Ile Trp Trp Val Ile 305 310 315 320 Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly Met Lys Trp Gly His Glu 325 330 335 Ala Ile Glu Ala Asn Ser Gln Tyr Phe His Leu Ala Ala Trp Ala Val 340 345 350 Pro Ala Ile Lys Thr Ile Thr Ile Leu Ala Leu Gly Gln Val Asp Gly 355 360 365 Asp Val Leu Ser Gly Val Cys Phe Val Gly Leu Asn Asn Val Asp Ala 370 375 380 Leu Arg Gly Phe Val Leu Ala Pro Leu Phe Val Tyr Leu Phe Ile Gly 385 390 395 400 Thr Ser Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Thr 405 410 415 Ile Met Lys His Asp Gly Thr Lys Thr Glu Lys Leu Glu Lys Leu Met 420 425 430 Val Arg Ile Gly Val Phe Ser Val Leu Tyr Thr Val Pro Ala Thr Ile 435 440 445 Val Ile Ala Cys Tyr Phe Tyr Glu Gln Ala Phe Arg Asp Gln Trp Glu 450 455 460 Arg Ser Trp Val Ala Gln Ser Cys Lys Ser Tyr Ala Ile Pro Cys Pro 465 470 475 480 His Leu Gln Gly Gly Gly Gly Val Pro Pro His Pro Pro Met Ser Pro 485 490 495 Asp Phe Thr Val Phe Met Ile Lys Tyr Leu Met Thr Leu Ile Val Gly 500 505 510 Ile Thr Ser Gly Phe Trp Ile Trp Ser Gly Lys Thr Leu Asn Ser Trp 515 520 525 Arg Lys Phe Tyr Thr Arg Leu Thr Asn Ser Lys Gln Gly Glu Thr Thr 530 535 540 41 529 PRT Rat 41 Met Arg Ala Arg Ser Ala Leu Pro Arg Ser Ala Leu Pro Arg Leu Leu 1 5 10 15 Leu Pro Leu Leu Leu Leu Pro Ala Ala Gly Pro Ala Gln Phe His Gly 20 25 30 Glu Lys Gly Ile Ser Ile Pro Asp His Gly Phe Cys Gln Pro Ile Ser 35 40 45 Ile Pro Leu Cys Thr Asp Ile Ala Tyr Asn Gln Thr Ile Met Pro Asn 50 55 60 Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly Leu Glu Val His Gln 65 70 75 80 Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Pro Glu Leu Arg Phe Phe 85 90 95 Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val Leu Glu Gln Ala Ile 100 105 110 Pro Pro Cys Arg Ser Ile Cys Glu Arg Ala Arg Gln Gly Cys Glu Ala 115 120 125 Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Glu Arg Leu Arg Cys Glu 130 135 140 His Phe Pro Arg His Gly Ala Glu Gln Ile Cys Val Gly Gln Asn His 145 150 155 160 Ser Glu Asp Gly Thr Pro Ala Leu Leu Thr Thr Ala Pro Pro Ser Gly 165 170 175 Leu Gln Pro Gly Leu Gly Glu Arg Asp Cys Ala Ala Pro Cys Glu Pro 180 185 190 Ala Arg Pro Asp Gly Ser Met Phe Phe Ser His His His Thr Arg Phe 195 200 205 Ala Arg Leu Trp Ile Leu Thr Trp Ser Val Leu Cys Cys Ala Ser Thr 210 215 220 Phe Phe Thr Val Thr Thr Ser Leu Val Ala Met Gln Arg Phe Arg Tyr 225 230 235 240 Pro Glu Arg Pro Ile Ile Phe Leu Ser Gly Cys Tyr Thr Met Val Ser 245 250 255 Val Ala Tyr Ile Ala Gly Phe Val Leu Gln Glu Arg Val Val Cys Asn 260 265 270 Glu Arg Phe Ser Glu Asp Gly Tyr Arg Thr Val Gly Gln Gly Thr Lys 275 280 285 Lys Glu Gly Cys Thr Ile Leu Phe Met Met Leu Tyr Phe Phe Ser Met 290 295 300 Ala Ser Ser Ile Trp Trp Val Ile Leu Ser Leu Thr Trp Phe Leu Ala 305 310 315 320 Ala Gly Met Lys Trp Gly His Ala Ala Ile Glu Ala Asn Ser Gln Tyr 325 330 335 Phe His Leu Ala Ala Trp Ala Val Pro Ala Val Lys Thr Ile Thr Ile 340 345 350 Leu Ala Met Gly Gln Ile Asp Gly Asp Leu Leu Ser Gly Val Cys Phe 355 360 365 Val Gly Leu Asn Arg Leu Asp Pro Leu Arg Gly Phe Val Leu Ala Pro 370 375 380 Leu Phe Val Tyr Leu Phe Ile Gly Thr Ser Phe Leu Leu Ala Gly Phe 385 390 395 400 Val Ser Leu Phe Arg Ile Arg Thr Ile Met Lys His Asp Gly Thr Lys 405 410 415 Thr Glu Pro Leu Glu Arg Leu Met Val Arg Ile Gly Val Phe Ser Val 420 425 430 Leu Tyr Thr Val Pro Ala Thr Ile Val Ile Ala Cys Tyr Phe Tyr Glu 435 440 445 Gln Ala Phe Arg Glu His Trp Glu Arg Ser Trp Val Ser Gln His Cys 450 455 460 Lys Ser Leu Ala Ile Pro Cys Pro Ala His Tyr Thr Pro Arg Thr Ser 465 470 475 480 Pro Asp Phe Thr Val Tyr Met Ile Lys Tyr Leu Met Thr Leu Ile Val 485 490 495 Gly Ile Thr Ser Gly Phe Trp Ile Trp Ser Gly Lys Thr Leu His Ser 500 505 510 Trp Arg Lys Phe Tyr Thr Arg Leu Thr Asn Ser Arg His Gly Glu Thr 515 520 525 Thr 42 536 PRT Drosophila 42 Ile Leu Pro Thr Leu Ile Gln Gly Val Gln Arg Tyr Asp Gln Ser Pro 1 5 10 15 Leu Asp Ala Ser Pro Tyr Tyr Arg Ser Gly Gly Gly Leu Met Ala Ser 20 25 30 Ser Gly Thr Glu Leu Asp Gly Leu Pro His His Asn Arg Cys Glu Pro 35 40 45 Ile Thr Ile Ser Ile Cys Lys Asn Ile Pro Tyr Asn Met Thr Ile Met 50 55 60 Pro Asn Leu Ile Gly His Thr Lys Gln Glu Glu Ala Gly Leu Glu Val 65 70 75 80 His Gln Phe Ala Pro Leu Val Lys Ile Gly Cys Ser Asp Asp Leu Gln 85 90 95 Leu Phe Leu Cys Ser Leu Tyr Val Pro Val Cys Thr Ile Leu Glu Arg 100 105 110 Pro Ile Pro Pro Cys Arg Ser Leu Cys Glu Ser Ala Arg Val Cys Glu 115 120 125 Lys Leu Met Lys Thr Tyr Asn Phe Asn Trp Pro Glu Asn Leu Glu Cys 130 135 140 Ser Lys Phe Pro Val His Gly Gly Glu Asp Leu Cys Val Ala Glu Asn 145 150 155 160 Thr Thr Ser Ser Ala Ser Thr Ala Ala Thr Pro Thr Arg Ser Val Ala 165 170 175 Val Gly Gly Lys Asp Leu His Asp Cys Gly Ala Pro Cys His Ala Met 180 185 190 Phe Phe Pro Glu Arg Glu Arg Thr Val Leu Arg Tyr Trp Val Gly Ser 195 200 205 Trp Ala Ala Val Cys Val Ala Ser Cys Leu Phe Thr Val Leu Thr Phe 210 215 220 Leu Ile Asp Ser Ser Arg Phe Arg Tyr Pro Glu Arg Ala Ile Val Phe 225 230 235 240 Leu Ala Val Cys Tyr Leu Val Val Gly Cys Ala Tyr Val Ala Gly Leu 245 250 255 Gly Ala Gly Asp Ser Val Ser Cys Arg Glu Pro Phe Pro Pro Pro Val 260 265 270 Lys Leu Gly Arg Leu Gln Met Met Ser Thr Ile Thr Gln Gly His Arg 275 280 285 Gln Thr Thr Ser Cys Thr Val Leu Phe Met Ala Leu Tyr Phe Cys Cys 290 295 300 Met Ala Ala Phe Ala Trp Trp Ser Cys Leu Ala Phe Ala Trp Phe Leu 305 310 315 320 Ala Ala Gly Leu Lys Trp Gly His Glu Ala Ile Glu Asn Lys Ser His 325 330 335 Leu Phe His Leu Val Ala Trp Ala Val Pro Ala Leu Gln Thr Ile Ser 340 345 350 Val Leu Ala Leu Ala Lys Val Glu Gly Asp Ile Leu Ser Gly Val Cys 355 360 365 Phe Val Gly Gln Leu Asp Thr His Ser Leu Gly Ala Phe Leu Ile Leu 370 375 380 Pro Leu Cys Ile Tyr Leu Ser Ile Gly Ala Leu Phe Leu Leu Ala Gly 385 390 395 400 Phe Ile Ser Leu Phe Arg Ile Arg Thr Val Met Lys Thr Asp Gly Lys 405 410 415 Arg Thr Asp Lys Leu Glu Arg Leu Met Leu Arg Ile Gly Phe Phe Ser 420 425 430 Gly Leu Phe Ile Leu Pro Ala Val Gly Leu Leu Gly Cys Leu Phe Tyr 435 440 445 Glu Tyr Tyr Asn Phe Asp Glu Trp Met Ile Gln Trp His Arg Asp Ile 450 455 460 Cys Lys Pro Phe Ser Ile Pro Cys Pro Ala Ala Arg Ala Pro Gly Ser 465 470 475 480 Pro Glu Ala Arg Pro Ile Phe Gln Ile Phe Met Val Lys Tyr Leu Cys 485 490 495 Ser Met Leu Val Gly Val Thr Ser Ser Val Trp Leu Tyr Ser Ser Lys 500 505 510 Thr Met Val Ser Trp Arg Asn Phe Val Glu Arg Leu Gln Gly Lys Glu 515 520 525 Pro Arg Thr Arg Ala Gln Ala Tyr 530 535 43 570 PRT Drosophila 43 Gly Leu Val Leu Leu Leu Thr Ser Cys Arg Ala Asp Gly Pro Leu His 1 5 10 15 Ser Ala Asp His Gly Met Gly Gly Met Gly Met Gly Gly His Gly Leu 20 25 30 Asp Ala Ser Pro Ala Pro Gly Tyr Gly Val Pro Ala Ile Pro Lys Asp 35 40 45 Pro Asn Leu Arg Cys Glu Glu Ile Thr Ile Pro Met Cys Arg Gly Ile 50 55 60 Gly Tyr Asn Met Thr Ser Phe Pro Asn Glu Met Asn His Glu Thr Gln 65 70 75 80 Asp Glu Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile 85 90 95 Lys Cys Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro 100 105 110 Ile Cys Leu Glu Asp Tyr His Lys Pro Leu Pro Val Cys Arg Ser Val 115 120 125 Cys Glu Arg Ala Arg Ser Gly Cys Ala Pro Ile Met Gln Gln Tyr Ser 130 135 140 Phe Glu Trp Pro Glu Arg Met Ala Cys Glu His Leu Pro Leu His Gly 145 150 155 160 Asp Pro Asp Asn Leu Cys Met Glu Gln Pro Ser Tyr Thr Glu Ala Gly 165 170 175 Ser Gly Gly Ser Ser Gly Gly Ser Gly Gly Ser Gly Ser Gly Ser Gly 180 185 190 Ser Gly Gly Lys Arg Lys Gln Gly Gly Ser Gly Ser Gly Gly Ser Gly 195 200 205 Ala Gly Gly Ser Ser Gly Ser Thr Ser Thr Lys Pro Cys Arg Gly Arg 210 215 220 Gln Arg Ile Ala Gly Val Pro Asn Cys Gly Ile Pro Cys Lys Gly Pro 225 230 235 240 Phe Phe Ser Asn Asp Glu Lys Asp Phe Ala Gly Leu Trp Ile Ala Leu 245 250 255 Trp Ser Gly Leu Cys Phe Cys Ser Thr Leu Met Thr Leu Thr Thr Phe 260 265 270 Ile Ile Asp Thr Glu Arg Phe Lys Tyr Pro Glu Arg Pro Ile Val Phe 275 280 285 Leu Ser Ala Cys Tyr Phe Met Val Ala Val Gly Tyr Leu Ser Arg Asn 290 295 300 Phe Leu Gln Asn Glu Glu Ile Ala Cys Asp Gly Leu Leu Leu Arg Glu 305 310 315 320 Ser Ser Thr Gly Pro His Ser Cys Thr Leu Val Phe Leu Leu Thr Tyr 325 330 335 Phe Phe Gly Met Ala Ser Ser Ile Trp Trp Val Ile Leu Thr Phe Thr 340 345 350 Trp Phe Leu Ala Ala Gly Leu Lys Trp Gly Asn Glu Ala Ile Thr Lys 355 360 365 His Ser Gln Tyr Phe His Leu Ala Ala Trp Leu Ile Pro Thr Val Gln 370 375 380 Ser Val Ala Val Leu Leu Leu Ser Ala Val Asp Gly Asp Pro Ile Leu 385 390 395 400 Gly Ile Cys Tyr Val Gly Asn Leu Asn Pro Asp His Leu Lys Thr Phe 405 410 415 Val Leu Ala Pro Leu Phe Val Tyr Leu Val Ile Gly Thr Thr Phe Leu 420 425 430 Met Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Ser Val Ile Lys Gln 435 440 445 Gln Gly Gly Val Gly Ala Gly Val Lys Ala Asp Lys Leu Glu Lys Leu 450 455 460 Met Ile Arg Ile Gly Ile Phe Ser Val Leu Tyr Thr Val Pro Ala Thr 465 470 475 480 Ile Val Ile Gly Cys Tyr Leu Tyr Glu Ala Ala Tyr Phe Glu Asp Trp 485 490 495 Ile Lys Ala Leu Ala Cys Pro Cys Ala Gln Val Lys Gly Pro Gly Lys 500 505 510 Lys Pro Leu Tyr Ser Val Leu Met Leu Lys Tyr Phe Met Ala Leu Ala 515 520 525 Val Gly Ile Thr Ser Gly Val Trp Ile Trp Ser Gly Lys Thr Leu Glu 530 535 540 Ser Trp Arg Arg Phe Trp Arg Arg Leu Leu Gly Ala Pro Asp Arg Thr 545 550 555 560 Gly Ala Asn Gln Ala Leu Ile Lys Gln Arg 565 570 44 647 PRT Homo sapiens 44 Met Ala Glu Glu Glu Ala Pro Lys Lys Ser Arg Ala Ala Gly Gly Gly 1 5 10 15 Ala Ser Trp Glu Leu Cys Ala Gly Ala Leu Ser Ala Arg Leu Ala Glu 20 25 30 Glu Gly Ser Gly Asp Ala Gly Gly Arg Arg Arg Pro Pro Val Asp Pro 35 40 45 Arg Arg Leu Ala Arg Gln Leu Leu Leu Leu Leu Trp Leu Leu Glu Ala 50 55 60 Pro Leu Leu Leu Gly Val Arg Ala Gln Ala Ala Gly Gln Gly Pro Gly 65 70 75 80 Gln Gly Pro Gly Pro Gly Gln Gln Pro Pro Pro Pro Pro Gln Gln Gln 85 90 95 Gln Ser Gly Gln Gln Tyr Asn Gly Glu Arg Gly Ile Ser Val Pro Asp 100 105 110 His Gly Tyr Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala 115 120 125 Tyr Asn Gln Thr Ile Met Pro Asn Leu Leu Gly His Thr Asn Gln Glu 130 135 140 Asp Ala Gly Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln 145 150 155 160 Cys Ser Ala Glu Leu Lys Phe Phe Leu Cys Ser Met Tyr Ala Pro Val 165 170 175 Cys Thr Val Leu Glu Gln Ala Leu Pro Pro Cys Arg Ser Leu Cys Glu 180 185 190 Arg Ala Arg Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln 195 200 205 Trp Pro Asp Thr Leu Lys Cys Glu Lys Phe Pro Val His Gly Ala Gly 210 215 220 Glu Leu Cys Val Gly Gln Asn Thr Ser Asp Lys Gly Thr Pro Thr Pro 225 230 235 240 Ser Leu Leu Pro Glu Phe Trp Thr Ser Asn Pro Gln His Gly Gly Gly 245 250 255 Gly His Arg Gly Gly Phe Pro Gly Gly Ala Gly Ala Ser Glu Arg Gly 260 265 270 Lys Phe Ser Cys Pro Arg Ala Leu Lys Val Pro Ser Tyr Leu Asn Tyr 275 280 285 His Phe Leu Gly Glu Lys Asp Cys Gly Ala Pro Cys Glu Pro Thr Lys 290 295 300 Val Tyr Gly Leu Met Tyr Phe Gly Pro Glu Glu Leu Arg Phe Ser Arg 305 310 315 320 Thr Trp Ile Gly Ile Trp Ser Val Leu Cys Cys Ala Ser Thr Leu Phe 325 330 335 Thr Val Leu Thr Tyr Leu Val Asp Met Arg Arg Phe Ser Tyr Pro Glu 340 345 350 Arg Pro Ile Ile Phe Leu Ser Gly Cys Tyr Thr Ala Val Ala Val Ala 355 360 365 Tyr Ile Ala Gly Phe Leu Leu Glu Asp Arg Val Val Cys Asn Asp Lys 370 375 380 Phe Ala Glu Asp Gly Ala Arg Thr Val Ala Gln Gly Thr Lys Lys Glu 385 390 395 400 Gly Cys Thr Ile Leu Phe Met Met Leu Tyr Phe Phe Ser Met Ala Ser 405 410 415 Ser Ile Trp Trp Val Ile Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly 420 425 430 Met Lys Trp Gly His Glu Ala Ile Glu Ala Asn Ser Gln Tyr Phe His 435 440 445 Leu Ala Ala Trp Ala Val Pro Ala Ile Lys Thr Ile Thr Ile Leu Ala 450 455 460 Leu Gly Gln Val Asp Gly Asp Val Leu Ser Gly Val Cys Phe Val Gly 465 470 475 480 Leu Asn Asn Val Asp Ala Leu Arg Gly Phe Val Leu Ala Pro Leu Phe 485 490 495 Val Tyr Leu Phe Ile Gly Thr Ser Phe Leu Leu Ala Gly Phe Val Ser 500 505 510 Leu Phe Arg Ile Arg Thr Ile Met Lys His Asp Gly Thr Lys Thr Glu 515 520 525 Lys Leu Glu Lys Leu Met Val Arg Ile Gly Val Phe Ser Val Leu Tyr 530 535 540 Thr Val Pro Ala Thr Ile Val Ile Ala Cys Tyr Phe Tyr Glu Gln Ala 545 550 555 560 Phe Arg Asp Gln Trp Glu Arg Ser Trp Val Ala Gln Ser Cys Lys Ser 565 570 575 Tyr Ala Ile Pro Cys Pro His Leu Gln Ala Gly Gly Gly Ala Pro Pro 580 585 590 His Pro Pro Met Ser Pro Asp Phe Thr Val Phe Met Ile Lys Tyr Leu 595 600 605 Met Thr Leu Ile Val Gly Ile Thr Ser Gly Phe Trp Ile Trp Ser Gly 610 615 620 Lys Thr Leu Asn Ser Trp Arg Lys Phe Tyr Thr Arg Leu Thr Asn Ser 625 630 635 640 Lys Gln Gly Glu Thr Thr Val 645 45 626 PRT Mouse 45 Met Ala Glu Glu Ala Ala Pro Ser Glu Ser Arg Ala Ala Gly Arg Leu 1 5 10 15 Ser Leu Glu Leu Cys Ala Glu Ala Leu Pro Gly Arg Arg Glu Glu Val 20 25 30 Gly His Glu Asp Thr Ala Ser His Arg Arg Pro Arg Ala Asp Pro Arg 35 40 45 Arg Trp Ala Ser Gly Leu Leu Leu Leu Leu Trp Leu Leu Glu Ala Pro 50 55 60 Leu Leu Leu Gly Val Arg Ala Gln Ala Ala Gly Gln Val Ser Gly Pro 65 70 75 80 Gly Gln Gln Ala Pro Pro Pro Pro Gln Pro Gln Gln Ser Gly Gln Gln 85 90 95 Tyr Asn Gly Glu Arg Gly Ile Ser Ile Pro Asp His Gly Tyr Cys Gln 100 105 110 Pro Ile Ser Ile Pro Leu Cys Thr Asp Met Ala Tyr Asn Gln Thr Ile 115 120 125 Met Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly Leu Glu 130 135 140 Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Ala Glu Leu 145 150 155 160 Lys Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val Leu Glu 165 170 175 Gln Ala Leu Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg Gln Gly 180 185 190 Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Asp Thr Leu 195 200 205 Lys Cys Glu Lys Phe Pro Val His Gly Ala Gly Glu Leu Cys Val Gly 210 215 220 Gln Asn Thr Ser Asp Lys Gly Thr Pro Thr Pro Ser Leu Leu Pro Glu 225 230 235 240 Phe Trp Thr Ser Asn Gly Gln His Gly Gly Gly Gly Tyr Arg Gly Gly 245 250 255 Tyr Pro Gly Gly Ala Gly Thr Val Glu Arg Gly Lys Phe Ser Cys Pro 260 265 270 Arg Ala Leu Arg Val Pro Ser Tyr Leu Asn Tyr His Phe Leu Gly Glu 275 280 285 Lys Asp Cys Gly Ala Pro Cys Glu Pro Thr Lys Val Tyr Gly Leu Met 290 295 300 Tyr Phe Gly Pro Glu Glu Leu Arg Phe Ser Arg Thr Trp Ile Gly Ile 305 310 315 320 Trp Ser Val Leu Cys Cys Ala Ser Thr Leu Phe Thr Val Leu Thr Tyr 325 330 335 Leu Val Asp Met Pro Arg Phe Ser Tyr Pro Glu Arg Pro Ile Ile Ser 340 345 350 Leu Ser Gly Cys Tyr Thr Ala Val Ala Val Ala Tyr Ile Ala Gly Phe 355 360 365 Leu Leu Glu Asp Arg Val Val Cys Asn Asp Lys Phe Ala Glu Asp Gly 370 375 380 Ala Arg Thr Val Ala Gln Gly Thr Asn Lys Glu Gly Cys Thr Ile Leu 385 390 395 400 Phe Met Met Leu Tyr Phe Phe Ser Met Ala Ser Ser Ile Trp Trp Val 405 410 415 Ile Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly Met Lys Trp Gly His 420 425 430 Glu Ala Ile Glu Ala Asn Ser Gln Tyr Phe His Leu Ala Ala Trp Ala 435 440 445 Val Pro Ala Ile Lys Thr Ile Thr Ile Leu Ala Leu Gly Gln Val Asp 450 455 460 Gly Asp Val Leu Ser Gly Val Cys Phe Leu Gly Leu Asn Asn Val Asp 465 470 475 480 Ala Leu Arg Gly Phe Val Leu Ala Pro Leu Phe Val Tyr Leu Phe Ile 485 490 495 Gly Thr Ser Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg 500 505 510 Thr Ile Met Lys His Asp Gly Thr Lys Thr Glu Lys Leu Glu Lys Leu 515 520 525 Met Val Arg Ile Gly Val Phe Ser Val Leu Tyr Thr Val Pro Ala Thr 530 535 540 Ile Val Ile Ala Cys Tyr Phe Tyr Glu Gln Ala Phe Arg Asp Gln Trp 545 550 555 560 Glu Arg Ser Trp Val Ala Gln Ser Cys Lys Ser Tyr Ala Ile Pro Cys 565 570 575 Pro His Leu Gln Gly Gly Gly Gly Val Pro Pro His Pro Pro Met Ser 580 585 590 Pro Asp Phe Thr Val Phe Met Ile Lys Tyr Leu Met Thr Leu Asn Ser 595 600 605 Trp Arg Lys Phe Tyr Thr Arg Leu Thr Asn Ser Lys Gln Gly Glu Thr 610 615 620 Thr Val 625 46 565 PRT Homo sapiens 46 Met Arg Pro Arg Ser Ala Leu Pro Arg Leu Leu Leu Pro Leu Leu Leu 1 5 10 15 Leu Pro Ala Ala Gly Pro Ala Gln Phe His Gly Glu Lys Gly Ile Ser 20 25 30 Ile Pro Asp His Gly Phe Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr 35 40 45 Asp Ile Ala Tyr Asn Gln Thr Ile Met Pro Asn Leu Leu Gly His Thr 50 55 60 Asn Gln Glu Asp Ala Gly Leu Glu Val His Gln Phe Tyr Pro Leu Val 65 70 75 80 Lys Val Gln Cys Ser Pro Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr 85 90 95 Ala Pro Val Cys Thr Val Leu Glu Gln Ala Ile Pro Pro Cys Arg Ser 100 105 110 Ile Cys Glu Arg Ala Arg Gln Gly Cys Glu Ala Leu Met Asn Lys Phe 115 120 125 Gly Phe Gln Trp Pro Glu Arg Leu Arg Cys Glu His Phe Pro Arg His 130 135 140 Gly Ala Glu Gln Ile Cys Val Gly Gln Asn His Ser Glu Asp Gly Ala 145 150 155 160 Pro Ala Leu Leu Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro Gly Ala 165 170 175 Gly Gly Thr Pro Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro Arg Tyr 180 185 190 Ala Thr Leu Glu His Pro Phe His Cys Pro Arg Val Leu Lys Val Pro 195 200 205 Ser Tyr Leu Ser Tyr Lys Phe Leu Gly Glu Arg Asp Cys Ala Ala Pro 210 215 220 Cys Glu Pro Ala Arg Pro Asp Gly Ser Met Phe Phe Ser Gln Glu Glu 225 230 235 240 Thr Arg Phe Ala Arg Leu Trp Ile Leu Thr Trp Ser Val Leu Cys Cys 245 250 255 Ala Ser Thr Phe Phe Thr Val Thr Thr Tyr Leu Val Asp Met Gln Arg 260 265 270 Phe Arg Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Gly Cys Tyr Thr 275 280 285 Met Val Ser Val Ala Tyr Ile Ala Gly Phe Val Leu Gln Glu Arg Val 290 295 300 Val Cys Asn Glu Arg Phe Ser Glu Asp Gly Tyr Arg Thr Val Val Gln 305 310 315 320 Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu Phe Met Met Leu Tyr Phe 325 330 335 Phe Ser Met Ala Ser Ser Ile Trp Trp Val Ile Leu Ser Leu Thr Trp 340 345 350 Phe Leu Ala Ala Gly Met Lys Trp Gly His Glu Ala Ile Glu Ala Asn 355 360 365 Ser Gln Tyr Phe His Leu Ala Ala Trp Ala Val Pro Ala Val Lys Thr 370 375 380 Ile Thr Ile Leu Ala Met Gly Gln Ile Asp Gly Asp Leu Leu Ser Gly 385 390 395 400 Val Cys Phe Val Gly Leu Asn Ser Leu Asp Pro Leu Arg Gly Phe Val 405 410 415 Leu Ala Pro Leu Phe Val Tyr Leu Phe Ile Gly Thr Ser Phe Leu Leu 420 425 430 Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Thr Ile Met Lys His Asp 435 440 445 Gly Thr Lys Thr Glu Lys Leu Glu Arg Leu Met Val Arg Ile Gly Val 450 455 460 Phe Ser Val Leu Tyr Thr Val Pro Ala Thr Ile Val Ile Ala Cys Tyr 465 470 475 480 Phe Tyr Glu Gln Ala Phe Arg Glu His Trp Glu Arg Ser Trp Val Ser 485 490 495 Gln His Cys Lys Ser Leu Ala Ile Pro Cys Pro Ala His Tyr Thr Pro 500 505 510 Arg Met Ser Pro Asp Phe Thr Val Tyr Met Ile Lys Tyr Leu Met Thr 515 520 525 Leu Ile Val Gly Ile Thr Ser Gly Phe Trp Ile Trp Ser Gly Lys Thr 530 535 540 Leu His Ser Trp Arg Lys Phe Tyr Thr Arg Leu Thr Asn Ser Arg His 545 550 555 560 Gly Glu Thr Thr Val 565 47 666 PRT Homo sapiens 47 Met Ala Met Thr Trp Ile Val Phe Ser Leu Trp Pro Leu Thr Val Phe 1 5 10 15 Met Gly His Ile Gly Gly His Ser Leu Phe Ser Cys Glu Pro Ile Thr 20 25 30 Leu Arg Met Cys Gln Asp Leu Pro Tyr Asn Thr Thr Phe Met Pro Asn 35 40 45 Leu Leu Asn His Tyr Asp Gln Gln Thr Ala Ala Leu Ala Met Glu Pro 50 55 60 Phe His Pro Met Val Asn Leu Asp Cys Ser Arg Asp Phe Arg Pro Phe 65 70 75 80 Leu Cys Ala Leu Tyr Ala Pro Ile Cys Met Glu Tyr Gly Arg Val Thr 85 90 95 Leu Pro Cys Arg Arg Leu Cys Gln Arg Ala Tyr Ser Glu Cys Ser Lys 100 105 110 Leu Met Glu Met Phe Gly Val Pro Trp Pro Glu Asp Met Glu Cys Ser 115 120 125 Arg Phe Pro Asp Cys Asp Glu Pro Tyr Pro Arg Leu Val Asp Leu Asn 130 135 140 Leu Ala Gly Glu Pro Thr Glu Gly Ala Pro Val Ala Val Gln Arg Asp 145 150 155 160 Tyr Gly Phe Trp Cys Pro Arg Glu Leu Lys Ile Asp Pro Asp Leu Gly 165 170 175 Tyr Ser Phe Leu His Val Arg Asp Cys Ser Pro Pro Cys Pro Asn Met 180 185 190 Tyr Phe Arg Arg Glu Glu Leu Ser Phe Ala Arg Tyr Phe Ile Gly Leu 195 200 205 Ile Ser Ile Ile Cys Leu Ser Ala Thr Leu Phe Thr Phe Leu Thr Phe 210 215 220 Leu Ile Asp Val Thr Arg Phe Arg Tyr Pro Glu Arg Pro Ile Ile Phe 225 230 235 240 Tyr Ala Val Cys Tyr Met Met Val Ser Leu Ile Phe Phe Ile Gly Phe 245 250 255 Leu Leu Glu Asp Arg Val Ala Cys Asn Ala Ser Ile Pro Ala Gln Tyr 260 265 270 Lys Ala Ser Thr Val Thr Gln Gly Ser His Asn Lys Ala Cys Thr Met 275 280 285 Leu Phe Met Ile Leu Tyr Phe Phe Thr Met Ala Gly Ser Val Trp Trp 290 295 300 Val Ile Leu Thr Ile Thr Trp Phe Leu Ala Ala Val Pro Lys Trp Gly 305 310 315 320 Ser Glu Ala Ile Glu Lys Lys Ala Leu Leu Phe His Ala Ser Ala Trp 325 330 335 Gly Ile Pro Gly Thr Leu Thr Ile Ile Leu Leu Ala Met Asn Lys Ile 340 345 350 Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu Tyr Asp Val 355 360 365 Asp Ala Leu Arg Tyr Phe Val Leu Ala Pro Leu Cys Leu Tyr Val Val 370 375 380 Val Gly Val Ser Leu Leu Leu Ala Gly Ile Ile Ser Leu Asn Arg Val 385 390 395 400 Arg Ile Glu Ile Pro Leu Glu Lys Glu Asn Gln Asp Lys Leu Val Lys 405 410 415 Phe Met Ile Arg Ile Gly Val Phe Ser Ile Leu Tyr Leu Val Pro Leu 420 425 430 Leu Val Val Ile Gly Cys Tyr Phe Tyr Glu Gln Ala Tyr Arg Gly Ile 435 440 445 Trp Glu Thr Thr Trp Ile Gln Glu Arg Cys Arg Glu Tyr His Ile Pro 450 455 460 Cys Pro Tyr Gln Val Thr Gln Met Ser Arg Pro Asp Leu Ile Leu Phe 465 470 475 480 Leu Met Lys Tyr Leu Met Ala Leu Ile Val Gly Ile Pro Ser Val Phe 485 490 495 Trp Val Gly Ser Lys Lys Thr Cys Phe Glu Trp Ala Ser Phe Phe His 500 505 510 Gly Arg Arg Lys Lys Glu Ile Val Asn Glu Ser Arg Gln Val Leu Gln 515 520 525 Glu Pro Asp Phe Ala Gln Ser Leu Leu Arg Asp Pro Asn Thr Pro Ile 530 535 540 Ile Arg Lys Ser Arg Gly Thr Ser Thr Gln Gly Thr Ser Thr His Ala 545 550 555 560 Ser Ser Thr Gln Leu Ala Met Val Asp Asp Gln Arg Ser Lys Ala Gly 565 570 575 Ser Ile His Ser Lys Val Ser Ser Tyr His Gly Ser Leu His Arg Ser 580 585 590 Arg Asp Gly Arg Tyr Thr Pro Cys Ser Tyr Arg Gly Met Glu Glu Arg 595 600 605 Leu Pro His Gly Ser Met Ser Arg Leu Thr Asp His Ser Arg His Ser 610 615 620 Ser Ser His Arg Leu Asn Glu Gln Ser Arg His Ser Ser Ile Arg Asp 625 630 635 640 Leu Ser Asn Asn Pro Met Thr His Ile Thr His Gly Thr Ser Met Asn 645 650 655 Arg Val Ile Glu Glu Asp Gly Thr Ser Ala 660 665 48 666 PRT Mouse 48 Met Ala Val Ser Trp Ile Val Phe Asp Leu Trp Leu Leu Thr Val Phe 1 5 10 15 Leu Gly Gln Ile Gly Gly His Ser Leu Phe Ser Cys Glu Pro Ile Thr 20 25 30 Leu Arg Met Cys Gln Asp Leu Pro Tyr Asn Thr Thr Phe Met Pro Asn 35 40 45 Leu Leu Asn His Tyr Asp Gln Gln Thr Ala Ala Leu Ala Met Glu Pro 50 55 60 Phe His Pro Met Val Asn Leu Asp Cys Ser Arg Asp Phe Arg Pro Phe 65 70 75 80 Leu Cys Ala Leu Tyr Ala Pro Ile Cys Met Glu Tyr Gly Arg Val Thr 85 90 95 Leu Pro Cys Arg Arg Leu Cys Gln Arg Ala Tyr Ser Glu Cys Ser Lys 100 105 110 Leu Met Glu Met Phe Gly Val Pro Trp Pro Glu Asp Met Glu Cys Ser 115 120 125 Arg Phe Pro Asp Cys Asp Glu Pro Tyr Pro Arg Leu Val Asp Leu Asn 130 135 140 Leu Val Gly Asp Pro Thr Glu Gly Ala Pro Val Ala Val Gln Arg Asp 145 150 155 160 Tyr Gly Phe Trp Cys Pro Arg Glu Leu Lys Ile Asp Pro Asp Leu Gly 165 170 175 Tyr Ser Phe Leu His Val Arg Asp Cys Ser Pro Pro Cys Pro Asn Met 180 185 190 Tyr Phe Arg Arg Glu Glu Leu Ser Phe Ala Arg Tyr Phe Ile Gly Leu 195 200 205 Ile Ser Ile Ile Cys Leu Ser Ala Thr Leu Phe Thr Phe Leu Thr Phe 210 215 220 Leu Ile Asp Val Thr Arg Phe Arg Tyr Pro Glu Arg Pro Ile Ile Phe 225 230 235 240 Tyr Ala Val Cys Tyr Met Met Val Ser Leu Ile Phe Phe Ile Gly Phe 245 250 255 Leu Leu Glu Asp Arg Val Ala Cys Asn Ala Ser Ser Pro Ala Gln Tyr 260 265 270 Lys Ala Ser Thr Val Thr Gln Gly Ser His Asn Lys Ala Cys Thr Met 275 280 285 Leu Phe Met Val Leu Tyr Phe Phe Thr Met Ala Gly Ser Val Trp Trp 290 295 300 Val Ile Leu Thr Ile Thr Trp Phe Leu Ala Ala Val Pro Lys Trp Gly 305 310 315 320 Ser Glu Ala Ile Glu Lys Lys Ala Leu Leu Phe His Ala Ser Ala Trp 325 330 335 Gly Ile Pro Gly Thr Leu Thr Ile Ile Leu Leu Ala Met Asn Lys Ile 340 345 350 Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu Tyr Asp Val 355 360 365 Asp Ala Leu Arg Tyr Phe Val Leu Ala Pro Leu Cys Leu Tyr Val Val 370 375 380 Val Gly Val Ser Leu Leu Leu Ala Gly Ile Ile Ser Leu Asn Arg Val 385 390 395 400 Arg Ile Glu Ile Pro Leu Glu Lys Glu Asn Gln Asp Lys Leu Val Lys 405 410 415 Phe Met Ile Arg Ile Gly Val Phe Ser Ile Leu Tyr Leu Val Pro Leu 420 425 430 Leu Val Val Ile Gly Cys Tyr Phe Tyr Glu Gln Ala Tyr Arg Gly Ile 435 440 445 Trp Glu Thr Thr Trp Ile Gln Glu Arg Cys Arg Glu Tyr His Ile Pro 450 455 460 Cys Pro Tyr Gln Val Thr Gln Met Ser Arg Pro Asp Leu Ile Leu Phe 465 470 475 480 Leu Met Lys Tyr Leu Met Ala Leu Ile Val Gly Ile Pro Ser Ile Phe 485 490 495 Trp Val Gly Ser Lys Lys Thr Cys Phe Glu Trp Ala Ser Phe Phe His 500 505 510 Gly Arg Arg Lys Lys Glu Ile Val Asn Glu Ser Arg Gln Val Leu Gln 515 520 525 Glu Pro Asp Phe Ala Gln Ser Leu Leu Arg Asp Pro Asn Thr Pro Ile 530 535 540 Ile Arg Lys Ser Arg Gly Thr Ser Thr Gln Gly Thr Ser Thr His Ala 545 550 555 560 Ser Ser Thr Gln Leu Ala Met Val Asp Asp Gln Arg Ser Lys Ala Gly 565 570 575 Ser Val His Ser Lys Val Ser Ser Tyr His Gly Ser Leu His Arg Ser 580 585 590 Arg Asp Gly Arg Tyr Thr Pro Cys Ser Tyr Arg Gly Met Glu Glu Arg 595 600 605 Leu Pro His Gly Ser Met Ser Arg Leu Thr Asp His Ser Arg His Ser 610 615 620 Ser Ser His Arg Leu Asn Glu Gln Ser Arg His Ser Ser Ile Arg Asp 625 630 635 640 Leu Ser Asn Asn Pro Met Thr His Ile Thr His Gly Thr Ser Met Asn 645 650 655 Arg Val Ile Glu Glu Asp Gly Thr Ser Ala 660 665 49 537 PRT Homo sapiens 49 Met Ala Trp Arg Gly Ala Gly Pro Ser Val Pro Gly Ala Pro Gly Gly 1 5 10 15 Val Gly Leu Ser Leu Gly Leu Leu Leu Gln Leu Leu Leu Leu Leu Gly 20 25 30 Pro Ala Arg Gly Phe Gly Asp Glu Glu Glu Arg Arg Cys Asp Pro Ile 35 40 45 Arg Ile Ser Met Cys Gln Asn Leu Gly Tyr Asn Val Thr Lys Met Pro 50 55 60 Asn Leu Val Gly His Glu Leu Gln Thr Asp Ala Glu Leu Gln Leu Thr 65 70 75 80 Thr Phe Thr Pro Leu Ile Gln Tyr Gly Cys Ser Ser Gln Leu Gln Phe 85 90 95 Phe Leu Cys Ser Val Tyr Val Pro Met Cys Thr Glu Lys Ile Asn Ile 100 105 110 Pro Ile Gly Pro Cys Gly Gly Met Cys Leu Ser Val Lys Arg Arg Cys 115 120 125 Glu Pro Val Leu Lys Glu Phe Gly Phe Ala Trp Pro Glu Ser Leu Asn 130 135 140 Cys Ser Lys Phe Pro Pro Gln Asn Asp His Asn His Met Cys Met Glu 145 150 155 160 Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr Pro Ile Gln 165 170 175 Pro Gly Glu Glu Cys His Ser Val Gly Thr Asn Ser Asp Gln Tyr Ile 180 185 190 Trp Val Lys Arg Ser Leu Asn Cys Val Leu Lys Cys Gly Tyr Asp Ala 195 200 205 Gly Leu Tyr Ser Arg Ser Ala Lys Glu Phe Thr Asp Ile Trp Met Ala 210 215 220 Val Trp Ala Ser Leu Cys Phe Ile Ser Thr Ala Phe Thr Val Leu Thr 225 230 235 240 Phe Leu Ile Asp Ser Ser Arg Phe Ser Tyr Pro Glu Arg Pro Ile Ile 245 250 255 Phe Leu Ser Met Cys Tyr Asn Ile Tyr Ser Ile Ala Tyr Ile Val Arg 260 265 270 Leu Thr Val Gly Arg Glu Arg Ile Ser Cys Asp Phe Glu Glu Ala Ala 275 280 285 Glu Pro Val Leu Ile Gln Glu Gly Leu Lys Asn Thr Gly Cys Ala Ile 290 295 300 Ile Phe Leu Leu Met Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp 305 310 315 320 Val Ile Leu Thr Leu Thr Trp Phe Leu Ala Ala Gly Leu Lys Trp Gly 325 330 335 His Glu Ala Ile Glu Met His Ser Ser Tyr Phe His Ile Ala Ala Trp 340 345 350 Ala Ile Pro Ala Val Lys Thr Ile Val Ile Leu Ile Met Arg Leu Val 355 360 365 Asp Ala Asp Glu Leu Thr Gly Leu Cys Tyr Val Gly Asn Gln Asn Leu 370 375 380 Asp Ala Leu Thr Gly Phe Val Val Ala Pro Leu Phe Thr Tyr Leu Val 385 390 395 400 Ile Gly Thr Leu Phe Ile Ala Ala Gly Leu Val Ala Leu Phe Lys Ile 405 410 415 Arg Ser Asn Leu Gln Lys Asp Gly Thr Lys Thr Asp Lys Leu Glu Arg 420 425 430 Leu Met Val Lys Ile Gly Val Phe Ser Val Leu Tyr Thr Val Pro Ala 435 440 445 Thr Cys Val Ile Ala Cys Tyr Phe Tyr Glu Ile Ser Asn Trp Ala Leu 450 455 460 Phe Arg Tyr Ser Ala Asp Asp Ser Asn Met Ala Val Glu Met Leu Lys 465 470 475 480 Ile Phe Met Ser Leu Leu Val Gly Ile Thr Ser Gly Met Trp Ile Trp 485 490 495 Ser Ala Lys Thr Leu His Thr Trp Gln Lys Cys Ser Asn Arg Leu Val 500 505 510 Asn Ser Gly Lys Val Lys Arg Glu Lys Arg Gly Asn Gly Trp Val Lys 515 520 525 Pro Gly Lys Gly Ser Glu Thr Val Val 530 535 50 537 PRT Mouse 50 Met Ala Trp Pro Gly Thr Gly Pro Ser Ser Arg Gly Ala Pro Gly Gly 1 5 10 15 Val Gly Leu Arg Leu Gly Leu Leu Leu Gln Phe Leu Leu Leu Leu Arg 20 25 30 Pro Thr Leu Gly Phe Gly Asp Glu Glu Glu Arg Arg Cys Asp Pro Ile 35 40 45 Arg Ile Ala Met Cys Gln Asn Leu Gly Tyr Asn Val Thr Lys Met Pro 50 55 60 Asn Leu Val Gly His Glu Leu Gln Thr Asp Ala Glu Leu Gln Leu Thr 65 70 75 80 Thr Phe Thr Pro Leu Ile Gln Tyr Gly Cys Ser Ser Gln Leu Gln Phe 85 90 95 Phe Leu Cys Ser Val Tyr Val Pro Met Cys Thr Glu Lys Ile Asn Ile 100 105 110 Pro Ile Gly Pro Cys Gly Gly Met Cys Leu Ser Val Lys Arg Arg Cys 115 120 125 Glu Pro Val Leu Arg Glu Phe Gly Phe Ala Trp Pro Asp Thr Leu Asn 130 135 140 Cys Ser Lys Phe Pro Pro Gln Asn Asp His Asn His Met Cys Met Glu 145 150 155 160 Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr Pro Ile Gln 165 170 175 Pro Gly Glu Glu Cys His Ser Val Gly Ser Asn Ser Asp Gln Tyr Ile 180 185 190 Trp Val Lys Arg Ser Leu Asn Cys Val Leu Lys Cys Gly Tyr Asp Ala 195 200 205 Gly Leu Tyr Ser Arg Ser Ala Lys Glu Phe Thr Asp Ile Trp Met Ala 210 215 220 Val Trp Ala Ser Leu Cys Phe Ile Ser Thr Thr Phe Thr Val Leu Thr 225 230 235 240 Phe Leu Ile Asp Ser Ser Arg Phe Ser Tyr Pro Glu Arg Pro Ile Ile 245 250 255 Phe Leu Ser Met Cys Tyr Asn Ile Tyr Ser Ile Ala Tyr Ile Val Arg 260 265 270 Leu Thr Val Gly Arg Glu Arg Ile Ser Cys Asp Phe Glu Glu Ala Ala 275 280 285 Glu Pro Val Leu Ile Gln Glu Gly Leu Lys Asn Thr Gly Cys Ala Ile 290 295 300 Ile Phe Leu Leu Met Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp 305 310 315 320 Val Ile Leu Thr Leu Thr Trp Phe Leu Ala Ala Gly Leu Lys Trp Gly 325 330 335 His Glu Ala Ile Glu Met His Ser Ser Tyr Phe His Ile Ala Ala Trp 340 345 350 Ala Ile Pro Ala Val Lys Thr Ile Val Ile Leu Ile Met Arg Leu Val 355 360 365 Asp Ala Asp Glu Leu Thr Gly Leu Cys Tyr Val Gly Asn Gln Asn Leu 370 375 380 Asp Ala Leu Thr Gly Phe Val Val Ala Pro Leu Phe Thr Tyr Leu Val 385 390 395 400 Ile Gly Thr Leu Phe Ile Ala Ala Gly Leu Val Ala Leu Phe Lys Ile 405 410 415 Arg Ser Asn Leu Gln Lys Asp Gly Thr Lys Thr Asp Lys Leu Glu Arg 420 425 430 Leu Met Val Lys Ile Gly Val Phe Ser Val Leu Tyr Thr Val Pro Ala 435 440 445 Thr Cys Val Ile Ala Cys Tyr Phe Tyr Glu Ile Ser Asn Trp Ala Leu 450 455 460 Phe Arg Tyr Ser Ala Asp Asp Ser Asn Met Ala Val Glu Met Leu Lys 465 470 475 480 Ile Phe Met Ser Leu Leu Val Gly Ile Thr Ser Gly Met Trp Ile Trp 485 490 495 Ser Ala Lys Thr Leu His Thr Trp Gln Lys Cys Ser Asn Arg Leu Val 500 505 510 Asn Ser Gly Lys Val Lys Arg Glu Lys Arg Gly Asn Gly Trp Val Lys 515 520 525 Pro Gly Lys Gly Asn Glu Thr Val Val 530 535 51 585 PRT Homo sapiens 51 Met Ala Arg Pro Asp Pro Ser Ala Pro Pro Ser Leu Leu Leu Leu Leu 1 5 10 15 Leu Ala Gln Leu Val Gly Arg Ala Ala Ala Ala Ser Lys Ala Pro Val 20 25 30 Cys Gln Glu Ile Thr Val Pro Met Cys Arg Gly Ile Gly Tyr Asn Leu 35 40 45 Thr His Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu Ala Gly 50 55 60 Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys Ser Pro 65 70 75 80 Asp Leu Arg Phe Phe Leu Cys Thr Met Tyr Thr Pro Ile Cys Leu Pro 85 90 95 Asp Tyr His Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu Arg Ala 100 105 110 Lys Ala Gly Cys Ser Pro Leu Met Arg Gln Tyr Gly Phe Ala Trp Pro 115 120 125 Glu Arg Met Ser Cys Asp Arg Leu Pro Val Leu Gly Arg Asp Ala Glu 130 135 140 Val Leu Cys Met Asp Tyr Asn Arg Ser Glu Ala Thr Thr Ala Pro Pro 145 150 155 160 Arg Pro Phe Pro Ala Lys Pro Thr Leu Pro Gly Pro Pro Gly Ala Pro 165 170 175 Ala Ser Gly Gly Glu Cys Pro Ala Gly Gly Pro Phe Val Cys Lys Cys 180 185 190 Arg Glu Pro Phe Val Pro Ile Leu Lys Glu Ser His Pro Leu Tyr Asn 195 200 205 Lys Val Arg Thr Gly Gln Val Pro Asn Cys Ala Val Pro Cys Tyr Gln 210 215 220 Pro Ser Phe Ser Ala Asp Glu Arg Thr Phe Ala Thr Phe Trp Ile Gly 225 230 235 240 Leu Trp Ser Val Leu Cys Phe Ile Ser Thr Ser Thr Thr Val Ala Thr 245 250 255 Phe Leu Ile Asp Met Asp Thr Phe Arg Tyr Pro Glu Arg Pro Ile Ile 260 265 270 Phe Leu Ser Ala Cys Tyr Leu Cys Val Ser Leu Gly Phe Leu Val Arg 275 280 285 Leu Val Val Gly His Ala Ser Val Ala Cys Ser Arg Glu His Asn His 290 295 300 Ile His Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr Ile Val Phe Leu 305 310 315 320 Leu Val Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp Val Ile Leu 325 330 335 Ser Leu Thr Trp Phe Leu Ala Ala Ala Met Lys Trp Gly Asn Glu Ala 340 345 350 Ile Ala Gly Tyr Gly Gln Tyr Phe His Leu Ala Ala Trp Leu Ile Pro 355 360 365 Ser Val Lys Ser Ile Thr Ala Leu Ala Leu Ser Ser Val Asp Gly Asp 370 375 380 Pro Val Ala Gly Ile Cys Tyr Val Gly Asn Gln Asn Leu Asn Ser Leu 385 390 395 400 Arg Arg Phe Val Leu Gly Pro Leu Val Leu Tyr Leu Leu Val Gly Thr 405 410 415 Leu Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Ser Val 420 425 430 Ile Lys Gln Gly Gly Thr Lys Thr Asp Lys Leu Glu Lys Leu Met Ile 435 440 445 Arg Ile Gly Ile Phe Thr Leu Leu Tyr Thr Val Pro Ala Ser Ile Val 450 455 460 Val Ala Cys Tyr Leu Tyr Glu Gln His Tyr Arg Glu Ser Trp Glu Ala 465 470 475 480 Ala Leu Thr Cys Ala Cys Pro Gly His Asp Thr Gly Gln Pro Arg Ala 485 490 495 Lys Pro Glu Tyr Trp Val Leu Met Leu Lys Tyr Phe Met Cys Leu Val 500 505 510 Val Gly Ile Thr Ser Gly Val Trp Ile Trp Ser Gly Lys Thr Val Glu 515 520 525 Ser Trp Arg Arg Phe Thr Ser Arg Cys Cys Cys Arg Pro Arg Arg Gly 530 535 540 His Lys Ser Gly Gly Ala Met Ala Ala Gly Asp Tyr Pro Glu Ala Ser 545 550 555 560 Ala Ala Leu Thr Gly Arg Thr Gly Pro Pro Gly Pro Ala Ala Thr Tyr 565 570 575 His Lys Gln Val Ser Leu Ser His Val 580 585 52 706 PRT Homo sapiens 52 Met Glu Met Phe Thr Phe Leu Leu Thr Cys Ile Phe Leu Pro Leu Leu 1 5 10 15 Arg Gly His Ser Leu Phe Thr Cys Glu Pro Ile Thr Val Pro Arg Cys 20 25 30 Met Lys Met Ala Tyr Asn Met Thr Phe Phe Pro Asn Leu Met Gly His 35 40 45 Tyr Asp Gln Ser Ile Ala Ala Val Glu Met Glu His Phe Leu Pro Leu 50 55 60 Ala Asn Leu Glu Cys Ser Pro Asn Ile Glu Thr Phe Leu Cys Lys Ala 65 70 75 80 Phe Val Pro Thr Cys Ile Glu Gln Ile His Val Val Pro Pro Cys Arg 85 90 95 Lys Leu Cys Glu Lys Val Tyr Ser Asp Cys Lys Lys Leu Ile Asp Thr 100 105 110 Phe Gly Ile Arg Trp Pro Glu Glu Leu Glu Cys Asp Arg Leu Gln Tyr 115 120 125 Cys Asp Glu Thr Val Pro Val Thr Phe Asp Pro His Thr Glu Phe Leu 130 135 140 Gly Pro Gln Lys Lys Thr Glu Gln Val Gln Arg Asp Ile Gly Phe Trp 145 150 155 160 Cys Pro Arg His Leu Lys Thr Ser Gly Gly Gln Gly Tyr Lys Phe Leu 165 170 175 Gly Ile Asp Gln Cys Ala Pro Pro Cys Pro Asn Met Tyr Phe Lys Ser 180 185 190 Asp Glu Leu Glu Phe Ala Lys Ser Phe Ile Gly Thr Val Ser Ile Phe 195 200 205 Cys Leu Cys Ala Thr Leu Phe Thr Phe Leu Thr Phe Leu Ile Asp Val 210 215 220 Arg Arg Phe Arg Tyr Pro Glu Arg Pro Ile Ile Tyr Tyr Ser Val Cys 225 230 235 240 Tyr Ser Ile Val Ser Leu Met Tyr Phe Ile Gly Phe Leu Leu Gly Asp 245 250 255 Ser Thr Ala Cys Asn Lys Ala Asp Glu Lys Leu Glu Leu Gly Asp Thr 260 265 270 Val Val Leu Gly Ser Gln Asn Lys Ala Cys Thr Val Leu Phe Met Leu 275 280 285 Leu Tyr Phe Phe Thr Met Ala Gly Thr Val Trp Trp Val Ile Leu Thr 290 295 300 Ile Thr Trp Phe Leu Ala Ala Gly Arg Lys Trp Ser Cys Glu Ala Ile 305 310 315 320 Glu Gln Lys Ala Val Trp Phe His Ala Val Ala Trp Gly Thr Pro Gly 325 330 335 Phe Leu Thr Val Met Leu Leu Ala Met Asn Lys Val Glu Gly Asp Asn 340 345 350 Ile Ser Gly Val Cys Phe Val Gly Leu Tyr Asp Leu Asp Ala Ser Arg 355 360 365 Tyr Phe Val Leu Leu Pro Leu Cys Leu Cys Val Phe Val Gly Leu Ser 370 375 380 Leu Leu Leu Ala Gly Ile Ile Ser Leu Asn His Val Arg Gln Val Ile 385 390 395 400 Gln His Asp Gly Arg Asn Gln Glu Lys Leu Lys Lys Phe Met Ile Arg 405 410 415 Ile Gly Val Phe Ser Gly Leu Tyr Leu Val Pro Leu Val Thr Leu Leu 420 425 430 Gly Cys Tyr Val Tyr Glu Gln Val Asn Arg Ile Thr Trp Glu Ile Thr 435 440 445 Trp Val Ser Asp His Cys Arg Gln Tyr His Ile Pro Cys Pro Tyr Gln 450 455 460 Ala Lys Ala Lys Ala Arg Pro Glu Leu Ala Leu Phe Met Ile Lys Tyr 465 470 475 480 Leu Met Thr Leu Ile Val Gly Ile Ser Ala Val Phe Trp Val Gly Ser 485 490 495 Lys Lys Thr Cys Thr Glu Trp Ala Gly Phe Phe Lys Arg Asn Arg Lys 500 505 510 Arg Asp Pro Ile Ser Glu Ser Arg Arg Val Leu Gln Glu Ser Cys Glu 515 520 525 Phe Phe Leu Lys His Asn Ser Lys Val Lys His Lys Lys Lys His Tyr 530 535 540 Lys Pro Ser Ser His Lys Leu Lys Val Ile Ser Lys Ser Met Gly Thr 545 550 555 560 Ser Thr Gly Ala Thr Ala Asn His Gly Thr Ser Ala Val Ala Ile Thr 565 570 575 Ser His Asp Tyr Leu Gly Gln Glu Thr Leu Thr Glu Ile Gln Thr Ser 580 585 590 Pro Glu Thr Ser Met Arg Glu Val Lys Ala Asp Gly Ala Ser Thr Pro 595 600 605 Arg Leu Arg Glu Gln Asp Cys Gly Glu Pro Ala Ser Pro Ala Ala Ser 610 615 620 Ile Ser Arg Leu Ser Gly Glu Gln Val Asp Gly Lys Gly Gln Ala Gly 625 630 635 640 Ser Val Ser Glu Ser Ala Arg Ser Glu Gly Arg Ile Ser Pro Lys Ser 645 650 655 Asp Ile Thr Asp Thr Gly Leu Ala Gln Ser Asn Asn Leu Gln Val Pro 660 665 670 Ser Ser Ser Glu Pro Ser Ser Leu Lys Gly Ser Thr Ser Leu Leu Val 675 680 685 His Pro Val Ser Gly Val Arg Lys Glu Gln Gly Gly Gly Cys His Ser 690 695 700 Asp Thr 705 53 709 PRT Mouse 53 Met Glu Arg Ser Pro Phe Leu Leu Ala Cys Ile Leu Leu Pro Leu Val 1 5 10 15 Arg Gly His Ser Leu Phe Thr Cys Glu Pro Ile Thr Val Pro Arg Cys 20 25 30 Met Lys Met Thr Tyr Asn Met Thr Phe Phe Pro Asn Leu Met Gly His 35 40 45 Tyr Asp Gln Gly Ile Ala Ala Val Glu Met Gly His Phe Leu His Leu 50 55 60 Ala Asn Leu Glu Cys Ser Pro Asn Ile Glu Met Phe Leu Cys Gln Ala 65 70 75 80 Phe Ile Pro Thr Cys Thr Glu Gln Ile His Val Val Leu Pro Cys Arg 85 90 95 Lys Leu Cys Glu Lys Ile Val Ser Asp Cys Lys Lys Leu Met Asp Thr 100 105 110 Phe Gly Ile Arg Trp Pro Glu Glu Leu Glu Cys Asn Arg Leu Pro His 115 120 125 Cys Asp Asp Thr Val Pro Val Thr Ser His Pro His Thr Glu Leu Ser 130 135 140 Gly Pro Gln Lys Lys Ser Asp Gln Val Pro Arg Asp Ile Gly Phe Trp 145 150 155 160 Cys Pro Lys His Leu Arg Thr Ser Gly Asp Gln Gly Tyr Arg Phe Leu 165 170 175 Gly Ile Glu Gln Cys Ala Pro Pro Cys Pro Asn Met Tyr Phe Lys Ser 180 185 190 Asp Glu Leu Asp Phe Ala Lys Ser Phe Ile Gly Ile Val Ser Ile Phe 195 200 205 Cys Leu Cys Ala Thr Leu Phe Thr Phe Leu Thr Phe Leu Ile Asp Val 210 215 220 Arg Arg Phe Arg Tyr Pro Glu Arg Pro Ile Ile Tyr Tyr Ser Val Cys 225 230 235 240 Tyr Ser Ile Val Ser Leu Met Tyr Phe Val Gly Phe Leu Leu Gly Asn 245 250 255 Ser Thr Ala Cys Asn Lys Ala Asp Glu Lys Leu Glu Leu Gly Asp Thr 260 265 270 Val Val Leu Gly Ser Lys Asn Lys Ala Cys Ser Val Val Phe Met Phe 275 280 285 Leu Tyr Phe Phe Thr Met Ala Gly Thr Val Trp Trp Val Ile Leu Thr 290 295 300 Ile Thr Trp Phe Leu Ala Ala Gly Arg Lys Trp Ser Cys Glu Ala Ile 305 310 315 320 Glu Gln Lys Ala Val Trp Phe His Ala Val Ala Trp Gly Ala Pro Gly 325 330 335 Phe Leu Thr Val Met Leu Leu Ala Met Asn Lys Val Glu Gly Asp Asn 340 345 350 Ile Ser Gly Val Cys Phe Val Gly Leu Tyr Asp Leu Asp Ala Ser Arg 355 360 365 Tyr Phe Val Leu Leu Pro Leu Cys Leu Cys Val Phe Val Gly Leu Ser 370 375 380 Leu Leu Leu Ala Gly Ile Ile Ser Leu Asn His Val Arg Gln Val Ile 385 390 395 400 Gln His Asp Gly Arg Asn Gln Glu Lys Leu Lys Lys Phe Met Ile Arg 405 410 415 Ile Gly Val Phe Ser Gly Leu Tyr Leu Val Pro Leu Val Thr Leu Leu 420 425 430 Gly Cys Tyr Val Tyr Glu Leu Val Asn Arg Ile Thr Trp Glu Met Thr 435 440 445 Trp Phe Ser Asp His Cys His Gln Tyr Arg Ile Pro Cys Pro Tyr Gln 450 455 460 Ala Asn Pro Lys Ala Arg Pro Glu Leu Ala Leu Phe Met Ile Lys Tyr 465 470 475 480 Leu Met Thr Leu Ile Val Gly Ile Ser Ala Val Phe Trp Val Gly Ser 485 490 495 Lys Lys Thr Cys Thr Glu Trp Ala Gly Phe Phe Lys Arg Asn Arg Lys 500 505 510 Arg Asp Pro Ile Ser Glu Ser Arg Arg Val Leu Gln Glu Ser Cys Glu 515 520 525 Phe Phe Leu Lys His Asn Ser Lys Val Lys His Lys Lys Lys His Gly 530 535 540 Ala Pro Gly Pro His Arg Leu Lys Val Ile Ser Lys Ser Met Gly Thr 545 550 555 560 Ser Thr Gly Ala Thr Thr Asn His Gly Thr Ser Ala Met Ala Ile Ala 565 570 575 Asp His Asp Tyr Leu Gly Gln Glu Thr Ser Thr Glu Val His Thr Ser 580 585 590 Pro Glu Ala Ser Val Lys Glu Gly Arg Ala Asp Arg Ala Asn Thr Pro 595 600 605 Ser Ala Lys Asp Arg Asp Cys Gly Glu Ser Ala Gly Pro Ser Ser Lys 610 615 620 Leu Ser Gly Asn Arg Asn Gly Arg Glu Ser Arg Ala Gly Gly Leu Lys 625 630 635 640 Glu Arg Ser Asn Gly Ser Glu Gly Ala Pro Ser Glu Gly Arg Val Ser 645 650 655 Pro Lys Ser Ser Val Pro Glu Thr Gly Leu Ile Asp Cys Ser Thr Ser 660 665 670 Gln Ala Ala Ser Ser Pro Glu Pro Thr Ser Leu Lys Gly Ser Thr Ser 675 680 685 Leu Pro Val His Ser Ala Ser Arg Ala Arg Lys Glu Gln Gly Ala Gly 690 695 700 Ser His Ser Asp Ala 705 54 574 PRT Homo sapiens 54 Met Arg Asp Pro Gly Ala Ala Ala Pro Leu Ser Ser Leu Gly Leu Cys 1 5 10 15 Ala Leu Val Leu Ala Leu Leu Gly Ala Leu Ser Ala Gly Ala Gly Ala 20 25 30 Gln Pro Tyr His Gly Glu Lys Gly Ile Ser Val Pro Asp His Gly Phe 35 40 45 Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala Tyr Asn Gln 50 55 60 Thr Ile Leu Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly 65 70 75 80 Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Pro 85 90 95 Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val 100 105 110 Leu Asp Gln Ala Ile Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg 115 120 125 Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Glu 130 135 140 Arg Leu Arg Cys Glu Asn Phe Pro Val His Gly Ala Gly Glu Ile Cys 145 150 155 160 Val Gly Gln Asn Thr Ser Asp Gly Ser Gly Gly Pro Gly Gly Gly Pro 165 170 175 Thr Ala Tyr Pro Thr Ala Pro Tyr Leu Pro Asp Leu Pro Phe Thr Ala 180 185 190 Leu Pro Pro Gly Ala Ser Asp Gly Arg Gly Arg Pro Ala Phe Pro Phe 195 200 205 Ser Cys Pro Arg Gln Leu Lys Val Pro Pro Tyr Leu Gly Tyr Arg Phe 210 215 220 Leu Gly Glu Arg Asp Cys Gly Ala Pro Cys Glu Pro Gly Arg Ala Asn 225 230 235 240 Gly Leu Met Tyr Phe Lys Glu Glu Glu Arg Arg Phe Ala Arg Leu Trp 245 250 255 Val Gly Val Trp Ser Val Leu Cys Cys Ala Ser Thr Leu Phe Thr Val 260 265 270 Leu Thr Tyr Leu Val Asp Met Arg Arg Phe Ser Tyr Pro Glu Arg Pro 275 280 285 Ile Ile Phe Leu Ser Gly Cys Tyr Phe Met Val Ala Val Ala His Val 290 295 300 Ala Gly Phe Leu Leu Glu Asp Arg Ala Val Cys Val Glu Arg Phe Ser 305 310 315 320 Asp Asp Gly Tyr Arg Thr Val Ala Gln Gly Thr Lys Lys Glu Gly Cys 325 330 335 Thr Ile Leu Phe Met Val Leu Tyr Phe Phe Gly Met Ala Ser Ser Ile 340 345 350 Trp Trp Val Ile Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly Met Lys 355 360 365 Trp Gly His Glu Ala Ile Glu Ala Asn Ser Gln Tyr Phe His Leu Ala 370 375 380 Ala Trp Ala Val Pro Ala Val Lys Thr Ile Thr Ile Leu Ala Met Gly 385 390 395 400 Gln Val Asp Gly Asp Leu Leu Ser Gly Val Cys Tyr Val Gly Leu Ser 405 410 415 Ser Val Asp Ala Leu Arg Gly Phe Val Leu Ala Pro Leu Phe Val Tyr 420 425 430 Leu Phe Ile Gly Thr Ser Phe Leu Leu Ala Gly Phe Val Ser Leu Phe 435 440 445 Arg Ile Arg Thr Ile Met Lys His Asp Gly Thr Lys Thr Glu Lys Leu 450 455 460 Glu Lys Leu Met Val Arg Ile Gly Val Phe Ser Val Leu Tyr Thr Val 465 470 475 480 Pro Ala Thr Ile Val Leu Ala Cys Tyr Phe Tyr Glu Gln Ala Phe Arg 485 490 495 Glu His Trp Glu Arg Thr Trp Leu Leu Gln Thr Cys Lys Ser Tyr Ala 500 505 510 Val Pro Cys Pro Pro Gly His Phe Pro Pro Met Ser Pro Asp Phe Thr 515 520 525 Val Phe Met Ile Lys Tyr Leu Met Thr Met Ile Val Gly Ile Thr Thr 530 535 540 Gly Phe Trp Ile Trp Ser Gly Lys Thr Leu Gln Ser Trp Arg Arg Phe 545 550 555 560 Tyr His Arg Leu Ser His Ser Ser Lys Gly Glu Thr Ala Val 565 570 55 572 PRT Mouse 55 Met Arg Gly Pro Gly Thr Ala Ala Ser His Ser Pro Leu Gly Leu Cys 1 5 10 15 Ala Leu Val Leu Ala Leu Leu Gly Ala Leu Pro Thr Asp Thr Arg Ala 20 25 30 Gln Pro Tyr His Gly Glu Lys Gly Ile Ser Val Pro Asp His Gly Phe 35 40 45 Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala Tyr Asn Gln 50 55 60 Thr Ile Leu Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly 65 70 75 80 Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Pro 85 90 95 Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val 100 105 110 Leu Asp Gln Ala Ile Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg 115 120 125 Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Glu 130 135 140 Arg Leu Arg Cys Glu Asn Phe Pro Val His Gly Ala Gly Glu Ile Cys 145 150 155 160 Val Gly Gln Asn Thr Ser Asp Gly Ser Gly Gly Ala Gly Gly Ser Pro 165 170 175 Thr Ala Tyr Pro Thr Ala Pro Tyr Leu Pro Asp Pro Pro Phe Thr Ala 180 185 190 Met Ser Pro Ser Asp Gly Arg Gly Arg Leu Ser Phe Pro Phe Ser Cys 195 200 205 Pro Arg Gln Leu Lys Val Pro Pro Tyr Leu Gly Tyr Arg Phe Leu Gly 210 215 220 Glu Arg Asp Cys Gly Ala Pro Cys Glu Pro Gly Arg Ala Asn Gly Leu 225 230 235 240 Met Tyr Phe Lys Glu Glu Glu Arg Arg Phe Ala Arg Leu Trp Val Gly 245 250 255 Val Trp Ser Val Leu Ser Cys Ala Ser Thr Leu Phe Thr Val Leu Thr 260 265 270 Tyr Leu Val Asp Met Arg Arg Phe Ser Tyr Pro Glu Arg Pro Ile Ile 275 280 285 Phe Leu Ser Gly Cys Tyr Phe Met Val Ala Val Ala His Val Ala Gly 290 295 300 Phe Leu Leu Glu Asp Arg Ala Val Cys Val Glu Arg Phe Ser Asp Asp 305 310 315 320 Gly Tyr Arg Thr Val Ala Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile 325 330 335 Leu Phe Met Val Leu Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp 340 345 350 Val Ile Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly Met Lys Trp Gly 355 360 365 His Glu Ala Ile Glu Ala Asn Ser Gln Tyr Phe His Leu Ala Ala Trp 370 375 380 Ala Val Pro Ala Val Lys Thr Ile Thr Ile Leu Ala Met Gly Gln Val 385 390 395 400 Asp Gly Asp Leu Leu Ser Gly Val Cys Tyr Val Gly Leu Ser Ser Val 405 410 415 Asp Ala Leu Arg Gly Phe Val Leu Ala Pro Leu Phe Val Tyr Leu Phe 420 425 430 Ile Gly Thr Ser Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile 435 440 445 Arg Thr Ile Met Lys His Asp Gly Thr Lys Thr Glu Lys Leu Glu Lys 450 455 460 Leu Met Val Arg Ile Gly Val Phe Ser Val Leu Tyr Thr Val Pro Ala 465 470 475 480 Thr Ile Val Leu Ala Cys Tyr Phe Tyr Glu Gln Ala Phe Arg Glu His 485 490 495 Trp Glu Arg Thr Trp Leu Leu Gln Thr Cys Lys Ser Tyr Ala Val Pro 500 505 510 Cys Pro Pro Arg His Phe Ser Pro Met Ser Pro Asp Phe Thr Val Phe 515 520 525 Met Ile Lys Tyr Leu Met Thr Met Ile Val Gly Ile Thr Thr Gly Phe 530 535 540 Trp Ile Trp Ser Gly Lys Thr Leu Gln Ser Trp Arg Arg Phe Tyr His 545 550 555 560 Arg Leu Ser His Ser Ser Lys Gly Glu Thr Ala Val 565 570 56 694 PRT Homo sapiens 56 Met Glu Trp Gly Tyr Leu Leu Glu Val Thr Ser Leu Leu Ala Ala Leu 1 5 10 15 Ala Leu Leu Gln Arg Ser Ser Gly Ala Ala Ala Ala Ser Ala Lys Glu 20 25 30 Leu Ala Cys Gln Glu Ile Thr Val Pro Leu Cys Lys Gly Ile Gly Tyr 35 40 45 Asn Tyr Thr Tyr Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu 50 55 60 Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys 65 70 75 80 Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro Ile Cys 85 90 95 Leu Glu Asp Tyr Lys Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu 100 105 110 Arg Ala Lys Ala Gly Cys Ala Pro Leu Met Arg Gln Tyr Gly Phe Ala 115 120 125 Trp Pro Asp Arg Met Arg Cys Asp Arg Leu Pro Glu Gln Gly Asn Pro 130 135 140 Asp Thr Leu Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala 145 150 155 160 Pro Ser Pro Pro Arg Arg Leu Pro Pro Pro Pro Pro Gly Glu Gln Pro 165 170 175 Pro Ser Gly Ser Gly His Gly Arg Pro Pro Gly Ala Arg Pro Pro His 180 185 190 Arg Gly Gly Gly Arg Gly Gly Gly Gly Gly Asp Ala Ala Ala Pro Pro 195 200 205 Ala Arg Gly Gly Gly Gly Gly Gly Lys Ala Arg Pro Pro Gly Gly Gly 210 215 220 Ala Ala Pro Cys Glu Pro Gly Cys Gln Cys Arg Ala Pro Met Val Ser 225 230 235 240 Val Ser Ser Glu Arg His Pro Leu Tyr Asn Arg Val Lys Thr Gly Gln 245 250 255 Ile Ala Asn Cys Ala Leu Pro Cys His Asn Pro Phe Phe Ser Gln Asp 260 265 270 Glu Arg Ala Phe Thr Val Phe Trp Ile Gly Leu Trp Ser Val Leu Cys 275 280 285 Phe Val Ser Thr Phe Ala Thr Val Ser Thr Phe Leu Ile Asp Met Glu 290 295 300 Arg Phe Lys Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Ala Cys Tyr 305 310 315 320 Leu Phe Val Ser Val Gly Tyr Leu Val Arg Leu Val Ala Gly His Glu 325 330 335 Lys Val Ala Cys Ser Gly Gly Ala Pro Gly Ala Gly Gly Ala Gly Gly 340 345 350 Ala Gly Gly Ala Ala Ala Gly Ala Gly Ala Ala Gly Ala Gly Ala Gly 355 360 365 Gly Pro Gly Gly Arg Gly Glu Tyr Glu Glu Leu Gly Ala Val Glu Gln 370 375 380 His Val Arg Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr Val Val Phe 385 390 395 400 Leu Leu Val Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp Val Ile 405 410 415 Leu Ser Leu Thr Trp Phe Leu Ala Ala Gly Met Lys Trp Gly Asn Glu 420 425 430 Ala Ile Ala Gly Tyr Ser Gln Tyr Phe His Leu Ala Ala Trp Leu Val 435 440 445 Pro Ser Val Lys Ser Ile Ala Val Leu Ala Leu Ser Ser Val Asp Gly 450 455 460 Asp Pro Val Ala Gly Ile Cys Tyr Val Gly Asn Gln Ser Leu Asp Asn 465 470 475 480 Leu Arg Gly Phe Val Leu Ala Pro Leu Val Ile Tyr Leu Phe Ile Gly 485 490 495 Thr Met Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Ser 500 505 510 Val Ile Lys Gln Gln Asp Gly Pro Thr Lys Thr His Lys Leu Glu Lys 515 520 525 Leu Met Ile Arg Leu Gly Leu Phe Thr Val Leu Tyr Thr Val Pro Ala 530 535 540 Ala Val Val Val Ala Cys Leu Phe Tyr Glu Gln His Asn Arg Pro Arg 545 550 555 560 Trp Glu Ala Thr His Asn Cys Pro Cys Leu Arg Asp Leu Gln Pro Asp 565 570 575 Gln Ala Arg Arg Pro Asp Tyr Ala Val Phe Met Leu Lys Tyr Phe Met 580 585 590 Cys Leu Val Val Gly Ile Thr Ser Gly Val Trp Val Trp Ser Gly Lys 595 600 605 Thr Leu Glu Ser Trp Arg Ser Leu Cys Thr Arg Cys Cys Trp Ala Ser 610 615 620 Lys Gly Ala Ala Val Gly Gly Gly Ala Gly Ala Thr Ala Ala Gly Gly 625 630 635 640 Gly Gly Gly Pro Gly Gly Gly Gly Gly Gly Gly Pro Gly Gly Gly Gly 645 650 655 Gly Pro Gly Gly Gly Gly Gly Ser Leu Tyr Ser Asp Val Ser Thr Gly 660 665 670 Leu Thr Trp Arg Ser Gly Thr Ala Ser Ser Val Ser Tyr Pro Lys Gln 675 680 685 Met Pro Leu Ser Gln Val 690 57 685 PRT Mouse 57 Met Glu Trp Gly Tyr Leu Leu Glu Val Thr Ser Leu Leu Ala Ala Leu 1 5 10 15 Ala Val Leu Gln Arg Ser Ser Gly Ala Ala Ala Ala Ser Ala Lys Glu 20 25 30 Leu Ala Cys Gln Glu Ile Thr Val Pro Leu Cys Lys Gly Ile Gly Tyr 35 40 45 Asn Tyr Thr Tyr Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu 50 55 60 Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys 65 70 75 80 Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro Ile Cys 85 90 95 Leu Glu Asp Tyr Lys Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu 100 105 110 Arg Ala Lys Ala Gly Cys Ala Pro Leu Met Arg Gln Tyr Gly Phe Ala 115 120 125 Trp Pro Asp Arg Met Arg Cys Asp Arg Leu Pro Glu Gln Gly Asn Pro 130 135 140 Asp Thr Leu Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala 145 150 155 160 Pro Ser Pro Pro Arg Arg Leu Pro Pro Pro Pro Pro Pro Gly Glu Gln 165 170 175 Pro Pro Ser Gly Ser Gly His Ser Arg Pro Pro Gly Ala Arg Pro Pro 180 185 190 His Arg Gly Gly Ser Ser Arg Gly Ser Gly Asp Ala Ala Ala Ala Pro 195 200 205 Pro Ser Arg Gly Gly Lys Ala Arg Pro Pro Gly Gly Gly Ala Ala Pro 210 215 220 Cys Glu Pro Gly Cys Gln Cys Arg Ala Pro Met Val Ser Val Ser Ser 225 230 235 240 Glu Arg His Pro Leu Tyr Asn Arg Val Lys Thr Gly Gln Ile Ala Asn 245 250 255 Cys Ala Leu Pro Cys His Asn Pro Phe Phe Ser Gln Asp Glu Arg Ala 260 265 270 Phe Thr Val Phe Trp Ile Gly Leu Trp Ser Val Leu Cys Phe Val Ser 275 280 285 Thr Phe Ala Thr Val Ser Thr Phe Leu Ile Asp Met Glu Arg Phe Lys 290 295 300 Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Ala Cys Tyr Leu Phe Val 305 310 315 320 Ser Val Gly Tyr Leu Val Arg Leu Val Ala Gly His Glu Lys Val Ala 325 330 335 Cys Ser Gly Gly Ala Pro Gly Ala Gly Gly Arg Gly Gly Ala Gly Gly 340 345 350 Ala Ala Ala Ala Gly Ala Gly Ala Ala Gly Arg Gly Ala Ser Ser Pro 355 360 365 Gly Ala Arg Gly Glu Tyr Glu Glu Leu Gly Ala Val Glu Gln His Val 370 375 380 Arg Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr Val Val Phe Leu Leu 385 390 395 400 Val Tyr Phe Phe Gly Met Ala Ser Ser Ile Trp Trp Val Ile Leu Ser 405 410 415 Leu Thr Trp Phe Leu Ala Ala Gly Met Lys Trp Gly Asn Glu Ala Ile 420 425 430 Ala Gly Tyr Ser Gln Tyr Phe His Leu Ala Ala Trp Leu Val Pro Ser 435 440 445 Val Lys Ser Ile Ala Val Leu Ala Leu Ser Ser Val Asp Gly Asp Pro 450 455 460 Val Ala Gly Ile Cys Tyr Val Gly Asn Gln Ser Leu Asp Asn Leu Arg 465 470 475 480 Gly Phe Val Leu Ala Pro Leu Val Ile Tyr Leu Phe Ile Gly Thr Met 485 490 495 Phe Leu Leu Ala Gly Phe Val Ser Leu Phe Arg Ile Arg Ser Val Ile 500 505 510 Lys Gln Gln Gly Gly Pro Thr Lys Thr His Lys Leu Glu Lys Leu Met 515 520 525 Ile Arg Leu Gly Leu Phe Thr Val Leu Tyr Thr Val Pro Ala Ala Val 530 535 540 Val Val Ala Cys Leu Phe Tyr Glu Gln His Asn Arg Pro Arg Trp Glu 545 550 555 560 Ala Thr His Asn Cys Pro Cys Leu Arg Asp Leu Gln Pro Asp Gln Ala 565 570 575 Arg Arg Pro Asp Tyr Ala Val Phe Met Leu Lys Tyr Phe Met Cys Leu 580 585 590 Val Val Gly Ile Thr Ser Gly Val Trp Val Trp Ser Gly Lys Thr Leu 595 600 605 Glu Ser Trp Arg Ala Leu Cys Thr Arg Cys Cys Trp Ala Ser Lys Gly 610 615 620 Ala Ala Val Gly Ala Gly Ala Gly Gly Ser Gly Pro Gly Gly Ser Gly 625 630 635 640 Pro Gly Pro Gly Gly Gly Gly Gly His Gly Gly Gly Gly Gly Ser Leu 645 650 655 Tyr Ser Asp Val Ser Thr Gly Leu Thr Trp Arg Ser Gly Thr Ala Ser 660 665 670 Ser Val Ser Tyr Pro Lys Gln Met Pro Leu Ser Gln Val 675 680 685 58 591 PRT Homo sapiens 58 Met Ala Val Ala Pro Leu Arg Gly Ala Leu Leu Leu Trp Gln Leu Leu 1 5 10 15 Ala Ala Gly Gly Ala Ala Leu Glu Ile Gly Arg Phe Asp Pro Glu Arg 20 25 30 Gly Arg Gly Ala Ala Pro Cys Gln Ala Val Glu Ile Pro Met Cys Arg 35 40 45 Gly Ile Gly Tyr Asn Leu Thr Arg Met Pro Asn Leu Leu Gly His Thr 50 55 60 Ser Gln Gly Glu Ala Ala Ala Glu Leu Ala Glu Phe Ala Pro Leu Val 65 70 75 80 Gln Tyr Gly Cys His Ser His Leu Arg Phe Phe Leu Cys Ser Leu Tyr 85 90 95 Ala Pro Met Cys Thr Asp Gln Val Ser Thr Pro Ile Pro Ala Cys Arg 100 105 110 Pro Met Cys Glu Gln Ala Arg Leu Arg Cys Ala Pro Ile Met Glu Gln 115 120 125 Phe Asn Phe Gly Trp Pro Asp Ser Leu Asp Cys Ala Arg Leu Pro Thr 130 135 140 Arg Asn Asp Pro His Ala Leu Cys Met Glu Ala Pro Glu Asn Ala Thr 145 150 155 160 Ala Gly Pro Ala Glu Pro His Lys Gly Leu Gly Met Leu Pro Val Ala 165 170 175 Pro Arg Pro Ala Arg Pro Pro Gly Asp Leu Gly Pro Gly Ala Gly Gly 180 185 190 Ser Gly Thr Cys Glu Asn Pro Glu Lys Phe Gln Tyr Val Glu Lys Ser 195 200 205 Arg Ser Cys Ala Pro Arg Cys Gly Pro Gly Val Glu Val Phe Trp Ser 210 215 220 Arg Arg Asp Lys Asp Phe Ala Leu Val Trp Met Ala Val Trp Ser Ala 225 230 235 240 Leu Cys Phe Phe Ser Thr Ala Phe Thr Val Leu Thr Phe Leu Leu Glu 245 250 255 Pro His Arg Phe Gln Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Met 260 265 270 Cys Tyr Asn Val Tyr Ser Leu Ala Phe Leu Ile Arg Ala Val Ala Gly 275 280 285 Ala Gln Ser Val Ala Cys Asp Gln Glu Ala Gly Ala Leu Tyr Val Ile 290 295 300 Gln Glu Gly Leu Glu Asn Thr Gly Cys Thr Leu Val Phe Leu Leu Leu 305 310 315 320 Tyr Tyr Phe Gly Met Ala Ser Ser Leu Trp Trp Val Val Leu Thr Leu 325 330 335 Thr Trp Phe Leu Ala Ala Gly Lys Lys Trp Gly His Glu Ala Ile Glu 340 345 350 Ala His Gly Ser Tyr Phe His Met Ala Ala Trp Gly Leu Pro Ala Leu 355 360 365 Lys Thr Ile Val Ile Leu Thr Leu Arg Lys Val Ala Gly Asp Glu Leu 370 375 380 Thr Gly Leu Cys Tyr Val Ala Ser Thr Asp Ala Ala Ala Leu Thr Gly 385 390 395 400 Phe Val Leu Val Pro Leu Ser Gly Tyr Leu Val Leu Gly Ser Ser Phe 405 410 415 Leu Leu Thr Gly Phe Val Ala Leu Phe His Ile Arg Lys Ile Met Lys 420 425 430 Thr Gly Gly Thr Asn Thr Glu Lys Leu Glu Lys Leu Met Val Lys Ile 435 440 445 Gly Val Phe Ser Ile Leu Tyr Thr Val Pro Ala Thr Cys Val Ile Val 450 455 460 Cys Tyr Val Tyr Glu Arg Leu Asn Met Asp Phe Trp Arg Leu Arg Ala 465 470 475 480 Thr Glu Gln Pro Cys Ala Ala Ala Ala Gly Pro Gly Gly Arg Arg Asp 485 490 495 Cys Ser Leu Pro Gly Gly Ser Val Pro Thr Val Ala Val Phe Met Leu 500 505 510 Lys Ile Phe Met Ser Leu Val Val Gly Ile Thr Ser Gly Val Trp Val 515 520 525 Trp Ser Ser Lys Thr Phe Gln Thr Trp Gln Ser Leu Cys Tyr Arg Lys 530 535 540 Ile Ala Ala Gly Arg Ala Arg Ala Lys Ala Cys Arg Ala Pro Gly Ser 545 550 555 560 Tyr Gly Arg Gly Thr His Cys His Tyr Lys Ala Pro Thr Val Val Leu 565 570 575 His Met Thr Lys Thr Asp Pro Ser Leu Glu Asn Pro Thr His Leu 580 585 590 59 591 PRT Mouse 59 Met Ala Val Pro Pro Leu Leu Arg Gly Ala Leu Leu Leu Trp Gln Leu 1 5 10 15 Leu Ala Thr Gly Gly Ala Ala Leu Glu Ile Gly Arg Phe Asp Pro Glu 20 25 30 Arg Gly Arg Gly Pro Ala Pro Cys Gln Ala Met Glu Ile Pro Met Cys 35 40 45 Arg Gly Ile Gly Tyr Asn Leu Thr Arg Met Pro Asn Leu Leu Gly His 50 55 60 Thr Ser Gln Gly Glu Ala Ala Ala Gln Leu Ala Glu Phe Ser Pro Leu 65 70 75 80 Val Gln Tyr Gly Cys His Ser His Leu Arg Phe Phe Leu Cys Ser Leu 85 90 95 Tyr Ala Pro Met Cys Thr Asp Gln Val Ser Thr Pro Ile Pro Ala Cys 100 105 110 Arg Pro Met Cys Glu Gln Ala Arg Leu Arg Cys Ala Pro Ile Met Glu 115 120 125 Gln Phe Asn Phe Gly Trp Pro Asp Ser Leu Asp Cys Ala Arg Leu Pro 130 135 140 Thr Arg Asn Asp Pro His Ala Leu Cys Met Glu Ala Pro Glu Asn Thr 145 150 155 160 Ala Gly Pro Thr Glu Pro His Lys Gly Leu Gly Met Leu Pro Val Ala 165 170 175 Pro Arg Pro Ala Arg Pro Pro Gly Asp Ser Ala Pro Gly Pro Gly Ser 180 185 190 Gly Gly Thr Cys Asp Asn Pro Glu Lys Phe Gln Tyr Val Glu Lys Ser 195 200 205 Arg Ser Cys Ala Pro Arg Cys Gly Pro Gly Val Glu Val Phe Trp Ser 210 215 220 Arg Arg Asp Lys Asp Phe Ala Leu Val Trp Met Ala Val Trp Ser Ala 225 230 235 240 Leu Cys Phe Phe Ser Thr Ala Phe Thr Val Phe Thr Phe Leu Leu Glu 245 250 255 Pro His Arg Phe Gln Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Met 260 265 270 Cys Tyr Asn Val Tyr Ser Leu Ala Phe Leu Ile Arg Ala Val Ala Gly 275 280 285 Ala Gln Ser Val Ala Cys Asp Gln Glu Ala Gly Ala Leu Tyr Val Ile 290 295 300 Gln Glu Gly Leu Glu Asn Thr Gly Cys Thr Leu Val Phe Leu Leu Leu 305 310 315 320 Tyr Tyr Phe Gly Met Ala Ser Ser Leu Trp Trp Val Val Leu Thr Leu 325 330 335 Thr Trp Phe Leu Ala Ala Gly Lys Lys Trp Gly His Glu Ala Ile Glu 340 345 350 Ala His Gly Ser Tyr Phe His Met Ala Ala Trp Gly Leu Pro Ala Leu 355 360 365 Lys Thr Ile Val Val Leu Thr Leu Arg Lys Val Ala Gly Asp Glu Leu 370 375 380 Thr Gly Leu Cys Tyr Val Ala Ser Met Asp Pro Ala Ala Leu Thr Gly 385 390 395 400 Phe Val Leu Val Pro Leu Ser Cys Tyr Leu Val Leu Gly Thr Ser Phe 405 410 415 Leu Leu Thr Gly Phe Val Ala Leu Phe His Ile Arg Lys Ile Met Lys 420 425 430 Thr Gly Gly Thr Asn Thr Glu Lys Leu Glu Lys Leu Met Val Lys Ile 435 440 445 Gly Val Phe Ser Ile Leu Tyr Thr Val Pro Ala Thr Cys Val Ile Val 450 455 460 Cys Tyr Val Tyr Glu Arg Leu Asn Met Asp Phe Trp Arg Leu Arg Ala 465 470 475 480 Thr Glu Gln Pro Cys Thr Ala Ala Thr Val Pro Gly Gly Arg Arg Asp 485 490 495 Cys Ser Leu Pro Gly Gly Ser Val Pro Thr Val Ala Val Phe Met Leu 500 505 510 Lys Ile Phe Met Ser Leu Val Val Gly Ile Thr Ser Gly Val Trp Val 515 520 525 Trp Ser Ser Lys Thr Phe Gln Thr Trp Gln Ser Leu Cys Tyr Arg Lys 530 535 540 Met Ala Ala Gly Arg Ala Arg Ala Lys Ala Cys Arg Thr Pro Gly Gly 545 550 555 560 Tyr Gly Arg Gly Thr His Cys His Tyr Lys Ala Pro Thr Val Val Leu 565 570 575 His Met Thr Lys Thr Asp Pro Ser Leu Glu Asn Pro Thr His Leu 580 585 590 60 581 PRT Homo sapiens Variant (464) Xaa = any amino acid 60 Met Gln Arg Pro Gly Pro Arg Leu Trp Leu Val Leu Gln Val Met Gly 1 5 10 15 Ser Cys Ala Ala Ile Ser Ser Met Asp Met Glu Arg Pro Gly Asp Gly 20 25 30 Lys Cys Gln Pro Ile Glu Ile Pro Met Cys Lys Asp Ile Gly Tyr Asn 35 40 45 Met Thr Arg Met Pro Asn Leu Met Gly His Glu Asn Gln Arg Glu Ala 50 55 60 Ala Ile Gln Leu His Glu Phe Ala Pro Leu Val Glu Tyr Gly Cys His 65 70 75 80 Gly His Leu Arg Phe Phe Leu Cys Ser Leu Tyr Ala Pro Met Cys Thr 85 90 95 Glu Gln Val Ser Thr Pro Ile Pro Ala Cys Arg Val Met Cys Glu Gln 100 105 110 Ala Arg Leu Lys Cys Ser Pro Ile Met Glu Gln Phe Asn Phe Lys Trp 115 120 125 Pro Asp Ser Leu Asp Cys Arg Lys Leu Pro Asn Lys Asn Asp Pro Asn 130 135 140 Tyr Leu Cys Met Glu Ala Pro Asn Asn Gly Ser Asp Glu Pro Thr Arg 145 150 155 160 Gly Ser Gly Leu Phe Pro Pro Leu Phe Arg Pro Gln Arg Pro His Ser 165 170 175 Ala Gln Glu His Pro Leu Lys Asp Gly Gly Pro Gly Arg Gly Gly Cys 180 185 190 Asp Asn Pro Gly Lys Phe His His Val Glu Lys Ser Ala Ser Cys Ala 195 200 205 Pro Leu Cys Thr Pro Gly Val Asp Val Tyr Trp Ser Arg Glu Asp Lys 210 215 220 Arg Phe Ala Val Val Trp Leu Ala Ile Trp Ala Val Leu Cys Phe Phe 225 230 235 240 Ser Ser Ala Phe Thr Val Leu Thr Phe Leu Ile Asp Pro Ala Arg Phe 245 250 255 Arg Tyr Pro Glu Arg Pro Ile Ile Phe Leu Ser Met Cys Tyr Cys Val 260 265 270 Tyr Ser Val Gly Tyr Leu Ile Arg Leu Phe Ala Gly Ala Glu Ser Ile 275 280 285 Ala Cys Asp Arg Asp Ser Gly Gln Leu Tyr Val Ile Gln Glu Gly Leu 290 295 300 Glu Ser Thr Gly Cys Thr Leu Val Phe Leu Val Leu Tyr Tyr Phe Gly 305 310 315 320 Met Ala Ser Ser Leu Trp Trp Val Val Leu Thr Leu Thr Trp Phe Leu 325 330 335 Ala Ala Gly Lys Lys Trp Gly His Glu Ala Ile Glu Ala Asn Ser Ser 340 345 350 Tyr Phe His Leu Ala Ala Trp Ala Ile Pro Ala Val Lys Thr Ile Leu 355 360 365 Ile Leu Val Met Arg Arg Val Ala Gly Asp Glu Leu Thr Gly Val Cys 370 375 380 Tyr Val Gly Ser Met Asp Val Asn Ala Leu Thr Gly Phe Val Leu Ile 385 390 395 400 Pro Leu Ala Cys Tyr Leu Val Ile Gly Thr Ser Phe Ile Leu Ser Gly 405 410 415 Phe Val Ala Leu Phe His Ile Arg Arg Val Met Lys Thr Gly Gly Glu 420 425 430 Asn Thr Asp Lys Leu Glu Lys Leu Met Val Arg Ile Gly Leu Phe Ser 435 440 445 Val Leu Tyr Thr Val Pro Ala Thr Cys Val Ile Ala Cys Tyr Phe Xaa 450 455 460 Glu His Leu Asn Met Asp Tyr Trp Lys Ile Leu Ala Ala Gln His Lys 465 470 475 480 Cys Lys Met Asn Asn Gln Thr Lys Thr Leu Asp Cys Leu Met Ala Ala 485 490 495 Ser Ile Pro Ala Val Glu Ile Phe Met Val Lys Ile Phe Met Leu Leu 500 505 510 Val Val Gly Ile Thr Ser Gly Met Trp Ile Trp Thr Ser Lys Thr Leu 515 520 525 Gln Ser Trp Gln Gln Val Cys Ser Arg Arg Leu Lys Lys Lys Ser Arg 530 535 540 Arg Lys Pro Ala Ser Val Ile Thr Ser Gly Gly Ile Tyr Lys Lys Ala 545 550 555 560 Gln His Pro Gln Lys Thr His His Gly Lys Tyr Glu Ile Pro Ala Gln 565 570 575 Ser Pro Thr Cys Val 580 61 319 PRT Homo sapiens 61 Met Ala Glu Glu Glu Ala Pro Lys Lys Ser Arg Ala Ala Gly Gly Gly 1 5 10 15 Ala Ser Trp Glu Leu Cys Ala Gly Ala Leu Ser Ala Arg Leu Ala Glu 20 25 30 Glu Gly Ser Gly Asp Ala Gly Gly Arg Arg Arg Pro Pro Val Asp Pro 35 40 45 Arg Arg Leu Ala Arg Gln Leu Leu Leu Leu Leu Trp Leu Leu Glu Ala 50 55 60 Pro Leu Leu Leu Gly Val Arg Ala Gln Ala Ala Gly Gln Gly Pro Gly 65 70 75 80 Gln Gly Pro Gly Pro Gly Gln Gln Pro Pro Pro Pro Pro Gln Gln Gln 85 90 95 Gln Ser Gly Gln Gln Tyr Asn Gly Glu Arg Gly Ile Ser Val Pro Asp 100 105 110 His Gly Tyr Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala 115 120 125 Tyr Asn Gln Thr Ile Met Pro Asn Leu Leu Gly His Thr Asn Gln Glu 130 135 140 Asp Ala Gly Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln 145 150 155 160 Cys Ser Ala Glu Leu Lys Phe Phe Leu Cys Ser Met Tyr Ala Pro Val 165 170 175 Cys Thr Val Leu Glu Gln Ala Leu Pro Pro Cys Arg Ser Leu Cys Glu 180 185 190 Arg Ala Arg Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln 195 200 205 Trp Pro Asp Thr Leu Lys Cys Glu Lys Phe Pro Val His Gly Ala Gly 210 215 220 Glu Leu Cys Val Gly Gln Asn Thr Ser Asp Lys Gly Thr Pro Thr Pro 225 230 235 240 Ser Leu Leu Pro Glu Phe Trp Thr Ser Asn Pro Gln His Gly Gly Gly 245 250 255 Gly His Arg Gly Gly Phe Pro Gly Gly Ala Gly Ala Ser Glu Arg Gly 260 265 270 Lys Phe Ser Cys Pro Arg Ala Leu Lys Val Pro Ser Tyr Leu Asn Tyr 275 280 285 His Phe Leu Gly Glu Lys Asp Cys Gly Ala Pro Cys Glu Pro Thr Lys 290 295 300 Val Tyr Gly Leu Met Tyr Phe Gly Pro Glu Glu Leu Arg Phe Ser 305 310 315 62 314 PRT Mouse 62 Met Ala Glu Glu Ala Ala Pro Ser Glu Ser Arg Ala Ala Gly Arg Leu 1 5 10 15 Ser Leu Glu Leu Cys Ala Glu Ala Leu Pro Gly Arg Arg Glu Glu Val 20 25 30 Gly His Glu Asp Thr Ala Ser His Arg Arg Pro Arg Ala Asp Pro Arg 35 40 45 Arg Trp Ala Ser Gly Leu Leu Leu Leu Leu Trp Leu Leu Glu Ala Pro 50 55 60 Leu Leu Leu Gly Val Arg Ala Gln Ala Ala Gly Gln Val Ser Gly Pro 65 70 75 80 Gly Gln Gln Ala Pro Pro Pro Pro Gln Pro Gln Gln Ser Gly Gln Gln 85 90 95 Tyr Asn Gly Glu Arg Gly Ile Ser Ile Pro Asp His Gly Tyr Cys Gln 100 105 110 Pro Ile Ser Ile Pro Leu Cys Thr Asp Met Ala Tyr Asn Gln Thr Ile 115 120 125 Met Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly Leu Glu 130 135 140 Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Ala Glu Leu 145 150 155 160 Lys Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val Leu Glu 165 170 175 Gln Ala Leu Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg Gln Gly 180 185 190 Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Asp Thr Leu 195 200 205 Lys Cys Glu Lys Phe Pro Val His Gly Ala Gly Glu Leu Cys Val Gly 210 215 220 Gln Asn Thr Ser Asp Lys Gly Thr Pro Thr Pro Ser Leu Leu Pro Glu 225 230 235 240 Phe Trp Thr Ser Asn Gly Gln His Gly Gly Gly Gly Tyr Arg Gly Gly 245 250 255 Tyr Pro Gly Gly Ala Gly Thr Val Glu Arg Gly Lys Phe Ser Cys Pro 260 265 270 Arg Ala Leu Arg Val Pro Ser Tyr Leu Asn Tyr His Phe Leu Gly Glu 275 280 285 Lys Asp Cys Gly Ala Pro Cys Glu Pro Thr Lys Val Tyr Gly Leu Met 290 295 300 Tyr Phe Gly Pro Glu Glu Leu Arg Phe Ser 305 310 63 244 PRT Homo sapiens 63 Met Arg Pro Arg Ser Ala Leu Pro Arg Leu Leu Leu Pro Leu Leu Leu 1 5 10 15 Leu Pro Ala Ala Gly Pro Ala Gln Phe His Gly Glu Lys Gly Ile Ser 20 25 30 Ile Pro Asp His Gly Phe Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr 35 40 45 Asp Ile Ala Tyr Asn Gln Thr Ile Met Pro Asn Leu Leu Gly His Thr 50 55 60 Asn Gln Glu Asp Ala Gly Leu Glu Val His Gln Phe Tyr Pro Leu Val 65 70 75 80 Lys Val Gln Cys Ser Pro Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr 85 90 95 Ala Pro Val Cys Thr Val Leu Glu Gln Ala Ile Pro Pro Cys Arg Ser 100 105 110 Ile Cys Glu Arg Ala Arg Gln Gly Cys Glu Ala Leu Met Asn Lys Phe 115 120 125 Gly Phe Gln Trp Pro Glu Arg Leu Arg Cys Glu His Phe Pro Arg His 130 135 140 Gly Ala Glu Gln Ile Cys Val Gly Gln Asn His Ser Glu Asp Gly Ala 145 150 155 160 Pro Ala Leu Leu Thr Thr Ala Pro Pro Pro Gly Leu Gln Pro Gly Ala 165 170 175 Gly Gly Thr Pro Gly Gly Pro Gly Gly Gly Gly Ala Pro Pro Arg Tyr 180 185 190 Ala Thr Leu Glu His Pro Phe His Cys Pro Arg Val Leu Lys Val Pro 195 200 205 Ser Tyr Leu Ser Tyr Lys Phe Leu Gly Glu Arg Asp Cys Ala Ala Pro 210 215 220 Cys Glu Pro Ala Arg Pro Asp Gly Ser Met Phe Phe Ser Gln Glu Glu 225 230 235 240 Thr Arg Phe Ala 64 202 PRT Homo sapiens 64 Met Ala Met Thr Trp Ile Val Phe Ser Leu Trp Pro Leu Thr Val Phe 1 5 10 15 Met Gly His Ile Gly Gly His Ser Leu Phe Ser Cys Glu Pro Ile Thr 20 25 30 Leu Arg Met Cys Gln Asp Leu Pro Tyr Asn Thr Thr Phe Met Pro Asn 35 40 45 Leu Leu Asn His Tyr Asp Gln Gln Thr Ala Ala Leu Ala Met Glu Pro 50 55 60 Phe His Pro Met Val Asn Leu Asp Cys Ser Arg Asp Phe Arg Pro Phe 65 70 75 80 Leu Cys Ala Leu Tyr Ala Pro Ile Cys Met Glu Tyr Gly Arg Val Thr 85 90 95 Leu Pro Cys Arg Arg Leu Cys Gln Arg Ala Tyr Ser Glu Cys Ser Lys 100 105 110 Leu Met Glu Met Phe Gly Val Pro Trp Pro Glu Asp Met Glu Cys Ser 115 120 125 Arg Phe Pro Asp Cys Asp Glu Pro Tyr Pro Arg Leu Val Asp Leu Asn 130 135 140 Leu Ala Gly Glu Pro Thr Glu Gly Ala Pro Val Ala Val Gln Arg Asp 145 150 155 160 Tyr Gly Phe Trp Cys Pro Arg Glu Leu Lys Ile Asp Pro Asp Leu Gly 165 170 175 Tyr Ser Phe Leu His Val Arg Asp Cys Ser Pro Pro Cys Pro Asn Met 180 185 190 Tyr Phe Arg Arg Glu Glu Leu Ser Phe Ala 195 200 65 202 PRT Mouse 65 Met Ala Val Ser Trp Ile Val Phe Asp Leu Trp Leu Leu Thr Val Phe 1 5 10 15 Leu Gly Gln Ile Gly Gly His Ser Leu Phe Ser Cys Glu Pro Ile Thr 20 25 30 Leu Arg Met Cys Gln Asp Leu Pro Tyr Asn Thr Thr Phe Met Pro Asn 35 40 45 Leu Leu Asn His Tyr Asp Gln Gln Thr Ala Ala Leu Ala Met Glu Pro 50 55 60 Phe His Pro Met Val Asn Leu Asp Cys Ser Arg Asp Phe Arg Pro Phe 65 70 75 80 Leu Cys Ala Leu Tyr Ala Pro Ile Cys Met Glu Tyr Gly Arg Val Thr 85 90 95 Leu Pro Cys Arg Arg Leu Cys Gln Arg Ala Tyr Ser Glu Cys Ser Lys 100 105 110 Leu Met Glu Met Phe Gly Val Pro Trp Pro Glu Asp Met Glu Cys Ser 115 120 125 Arg Phe Pro Asp Cys Asp Glu Pro Tyr Pro Arg Leu Val Asp Leu Asn 130 135 140 Leu Val Gly Asp Pro Thr Glu Gly Ala Pro Val Ala Val Gln Arg Asp 145 150 155 160 Tyr Gly Phe Trp Cys Pro Arg Glu Leu Lys Ile Asp Pro Asp Leu Gly 165 170 175 Tyr Ser Phe Leu His Val Arg Asp Cys Ser Pro Pro Cys Pro Asn Met 180 185 190 Tyr Phe Arg Arg Glu Glu Leu Ser Phe Ala 195 200 66 219 PRT Homo sapiens 66 Met Ala Trp Arg Gly Ala Gly Pro Ser Val Pro Gly Ala Pro Gly Gly 1 5 10 15 Val Gly Leu Ser Leu Gly Leu Leu Leu Gln Leu Leu Leu Leu Leu Gly 20 25 30 Pro Ala Arg Gly Phe Gly Asp Glu Glu Glu Arg Arg Cys Asp Pro Ile 35 40 45 Arg Ile Ser Met Cys Gln Asn Leu Gly Tyr Asn Val Thr Lys Met Pro 50 55 60 Asn Leu Val Gly His Glu Leu Gln Thr Asp Ala Glu Leu Gln Leu Thr 65 70 75 80 Thr Phe Thr Pro Leu Ile Gln Tyr Gly Cys Ser Ser Gln Leu Gln Phe 85 90 95 Phe Leu Cys Ser Val Tyr Val Pro Met Cys Thr Glu Lys Ile Asn Ile 100 105 110 Pro Ile Gly Pro Cys Gly Gly Met Cys Leu Ser Val Lys Arg Arg Cys 115 120 125 Glu Pro Val Leu Lys Glu Phe Gly Phe Ala Trp Pro Glu Ser Leu Asn 130 135 140 Cys Ser Lys Phe Pro Pro Gln Asn Asp His Asn His Met Cys Met Glu 145 150 155 160 Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr Pro Ile Gln 165 170 175 Pro Gly Glu Glu Cys His Ser Val Gly Thr Asn Ser Asp Gln Tyr Ile 180 185 190 Trp Val Lys Arg Ser Leu Asn Cys Val Leu Lys Cys Gly Tyr Asp Ala 195 200 205 Gly Leu Tyr Ser Arg Ser Ala Lys Glu Phe Thr 210 215 67 219 PRT Mouse 67 Met Ala Trp Pro Gly Thr Gly Pro Ser Ser Arg Gly Ala Pro Gly Gly 1 5 10 15 Val Gly Leu Arg Leu Gly Leu Leu Leu Gln Phe Leu Leu Leu Leu Arg 20 25 30 Pro Thr Leu Gly Phe Gly Asp Glu Glu Glu Arg Arg Cys Asp Pro Ile 35 40 45 Arg Ile Ala Met Cys Gln Asn Leu Gly Tyr Asn Val Thr Lys Met Pro 50 55 60 Asn Leu Val Gly His Glu Leu Gln Thr Asp Ala Glu Leu Gln Leu Thr 65 70 75 80 Thr Phe Thr Pro Leu Ile Gln Tyr Gly Cys Ser Ser Gln Leu Gln Phe 85 90 95 Phe Leu Cys Ser Val Tyr Val Pro Met Cys Thr Glu Lys Ile Asn Ile 100 105 110 Pro Ile Gly Pro Cys Gly Gly Met Cys Leu Ser Val Lys Arg Arg Cys 115 120 125 Glu Pro Val Leu Arg Glu Phe Gly Phe Ala Trp Pro Asp Thr Leu Asn 130 135 140 Cys Ser Lys Phe Pro Pro Gln Asn Asp His Asn His Met Cys Met Glu 145 150 155 160 Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr Pro Ile Gln 165 170 175 Pro Gly Glu Glu Cys His Ser Val Gly Ser Asn Ser Asp Gln Tyr Ile 180 185 190 Trp Val Lys Arg Ser Leu Asn Cys Val Leu Lys Cys Gly Tyr Asp Ala 195 200 205 Gly Leu Tyr Ser Arg Ser Ala Lys Glu Phe Thr 210 215 68 235 PRT Homo sapiens 68 Met Ala Arg Pro Asp Pro Ser Ala Pro Pro Ser Leu Leu Leu Leu Leu 1 5 10 15 Leu Ala Gln Leu Val Gly Arg Ala Ala Ala Ala Ser Lys Ala Pro Val 20 25 30 Cys Gln Glu Ile Thr Val Pro Met Cys Arg Gly Ile Gly Tyr Asn Leu 35 40 45 Thr His Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu Ala Gly 50 55 60 Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys Ser Pro 65 70 75 80 Asp Leu Arg Phe Phe Leu Cys Thr Met Tyr Thr Pro Ile Cys Leu Pro 85 90 95 Asp Tyr His Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu Arg Ala 100 105 110 Lys Ala Gly Cys Ser Pro Leu Met Arg Gln Tyr Gly Phe Ala Trp Pro 115 120 125 Glu Arg Met Ser Cys Asp Arg Leu Pro Val Leu Gly Arg Asp Ala Glu 130 135 140 Val Leu Cys Met Asp Tyr Asn Arg Ser Glu Ala Thr Thr Ala Pro Pro 145 150 155 160 Arg Pro Phe Pro Ala Lys Pro Thr Leu Pro Gly Pro Pro Gly Ala Pro 165 170 175 Ala Ser Gly Gly Glu Cys Pro Ala Gly Gly Pro Phe Val Cys Lys Cys 180 185 190 Arg Glu Pro Phe Val Pro Ile Leu Lys Glu Ser His Pro Leu Tyr Asn 195 200 205 Lys Val Arg Thr Gly Gln Val Pro Asn Cys Ala Val Pro Cys Tyr Gln 210 215 220 Pro Ser Phe Ser Ala Asp Glu Arg Thr Phe Ala 225 230 235 69 198 PRT Homo sapiens 69 Met Glu Met Phe Thr Phe Leu Leu Thr Cys Ile Phe Leu Pro Leu Leu 1 5 10 15 Arg Gly His Ser Leu Phe Thr Cys Glu Pro Ile Thr Val Pro Arg Cys 20 25 30 Met Lys Met Ala Tyr Asn Met Thr Phe Phe Pro Asn Leu Met Gly His 35 40 45 Tyr Asp Gln Ser Ile Ala Ala Val Glu Met Glu His Phe Leu Pro Leu 50 55 60 Ala Asn Leu Glu Cys Ser Pro Asn Ile Glu Thr Phe Leu Cys Lys Ala 65 70 75 80 Phe Val Pro Thr Cys Ile Glu Gln Ile His Val Val Pro Pro Cys Arg 85 90 95 Lys Leu Cys Glu Lys Val Tyr Ser Asp Cys Lys Lys Leu Ile Asp Thr 100 105 110 Phe Gly Ile Arg Trp Pro Glu Glu Leu Glu Cys Asp Arg Leu Gln Tyr 115 120 125 Cys Asp Glu Thr Val Pro Val Thr Phe Asp Pro His Thr Glu Phe Leu 130 135 140 Gly Pro Gln Lys Lys Thr Glu Gln Val Gln Arg Asp Ile Gly Phe Trp 145 150 155 160 Cys Pro Arg His Leu Lys Thr Ser Gly Gly Gln Gly Tyr Lys Phe Leu 165 170 175 Gly Ile Asp Gln Cys Ala Pro Pro Cys Pro Asn Met Tyr Phe Lys Ser 180 185 190 Asp Glu Leu Glu Phe Ala 195 70 198 PRT Mouse 70 Met Glu Arg Ser Pro Phe Leu Leu Ala Cys Ile Leu Leu Pro Leu Val 1 5 10 15 Arg Gly His Ser Leu Phe Thr Cys Glu Pro Ile Thr Val Pro Arg Cys 20 25 30 Met Lys Met Thr Tyr Asn Met Thr Phe Phe Pro Asn Leu Met Gly His 35 40 45 Tyr Asp Gln Gly Ile Ala Ala Val Glu Met Gly His Phe Leu His Leu 50 55 60 Ala Asn Leu Glu Cys Ser Pro Asn Ile Glu Met Phe Leu Cys Gln Ala 65 70 75 80 Phe Ile Pro Thr Cys Thr Glu Gln Ile His Val Val Leu Pro Cys Arg 85 90 95 Lys Leu Cys Glu Lys Ile Val Ser Asp Cys Lys Lys Leu Met Asp Thr 100 105 110 Phe Gly Ile Arg Trp Pro Glu Glu Leu Glu Cys Asn Arg Leu Pro His 115 120 125 Cys Asp Asp Thr Val Pro Val Thr Ser His Pro His Thr Glu Leu Ser 130 135 140 Gly Pro Gln Lys Lys Ser Asp Gln Val Pro Arg Asp Ile Gly Phe Trp 145 150 155 160 Cys Pro Lys His Leu Arg Thr Ser Gly Asp Gln Gly Tyr Arg Phe Leu 165 170 175 Gly Ile Glu Gln Cys Ala Pro Pro Cys Pro Asn Met Tyr Phe Lys Ser 180 185 190 Asp Glu Leu Asp Phe Ala 195 71 253 PRT Homo sapiens 71 Met Arg Asp Pro Gly Ala Ala Ala Pro Leu Ser Ser Leu Gly Leu Cys 1 5 10 15 Ala Leu Val Leu Ala Leu Leu Gly Ala Leu Ser Ala Gly Ala Gly Ala 20 25 30 Gln Pro Tyr His Gly Glu Lys Gly Ile Ser Val Pro Asp His Gly Phe 35 40 45 Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala Tyr Asn Gln 50 55 60 Thr Ile Leu Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly 65 70 75 80 Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Pro 85 90 95 Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val 100 105 110 Leu Asp Gln Ala Ile Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg 115 120 125 Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Glu 130 135 140 Arg Leu Arg Cys Glu Asn Phe Pro Val His Gly Ala Gly Glu Ile Cys 145 150 155 160 Val Gly Gln Asn Thr Ser Asp Gly Ser Gly Gly Pro Gly Gly Gly Pro 165 170 175 Thr Ala Tyr Pro Thr Ala Pro Tyr Leu Pro Asp Leu Pro Phe Thr Ala 180 185 190 Leu Pro Pro Gly Ala Ser Asp Gly Arg Gly Arg Pro Ala Phe Pro Phe 195 200 205 Ser Cys Pro Arg Gln Leu Lys Val Pro Pro Tyr Leu Gly Tyr Arg Phe 210 215 220 Leu Gly Glu Arg Asp Cys Gly Ala Pro Cys Glu Pro Gly Arg Ala Asn 225 230 235 240 Gly Leu Met Tyr Phe Lys Glu Glu Glu Arg Arg Phe Ala 245 250 72 251 PRT Mouse 72 Met Arg Gly Pro Gly Thr Ala Ala Ser His Ser Pro Leu Gly Leu Cys 1 5 10 15 Ala Leu Val Leu Ala Leu Leu Gly Ala Leu Pro Thr Asp Thr Arg Ala 20 25 30 Gln Pro Tyr His Gly Glu Lys Gly Ile Ser Val Pro Asp His Gly Phe 35 40 45 Cys Gln Pro Ile Ser Ile Pro Leu Cys Thr Asp Ile Ala Tyr Asn Gln 50 55 60 Thr Ile Leu Pro Asn Leu Leu Gly His Thr Asn Gln Glu Asp Ala Gly 65 70 75 80 Leu Glu Val His Gln Phe Tyr Pro Leu Val Lys Val Gln Cys Ser Pro 85 90 95 Glu Leu Arg Phe Phe Leu Cys Ser Met Tyr Ala Pro Val Cys Thr Val 100 105 110 Leu Asp Gln Ala Ile Pro Pro Cys Arg Ser Leu Cys Glu Arg Ala Arg 115 120 125 Gln Gly Cys Glu Ala Leu Met Asn Lys Phe Gly Phe Gln Trp Pro Glu 130 135 140 Arg Leu Arg Cys Glu Asn Phe Pro Val His Gly Ala Gly Glu Ile Cys 145 150 155 160 Val Gly Gln Asn Thr Ser Asp Gly Ser Gly Gly Ala Gly Gly Ser Pro 165 170 175 Thr Ala Tyr Pro Thr Ala Pro Tyr Leu Pro Asp Pro Pro Phe Thr Ala 180 185 190 Met Ser Pro Ser Asp Gly Arg Gly Arg Leu Ser Phe Pro Phe Ser Cys 195 200 205 Pro Arg Gln Leu Lys Val Pro Pro Tyr Leu Gly Tyr Arg Phe Leu Gly 210 215 220 Glu Arg Asp Cys Gly Ala Pro Cys Glu Pro Gly Arg Ala Asn Gly Leu 225 230 235 240 Met Tyr Phe Lys Glu Glu Glu Arg Arg Phe Ala 245 250 73 277 PRT Homo sapiens 73 Met Glu Trp Gly Tyr Leu Leu Glu Val Thr Ser Leu Leu Ala Ala Leu 1 5 10 15 Ala Leu Leu Gln Arg Ser Ser Gly Ala Ala Ala Ala Ser Ala Lys Glu 20 25 30 Leu Ala Cys Gln Glu Ile Thr Val Pro Leu Cys Lys Gly Ile Gly Tyr 35 40 45 Asn Tyr Thr Tyr Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu 50 55 60 Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys 65 70 75 80 Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro Ile Cys 85 90 95 Leu Glu Asp Tyr Lys Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu 100 105 110 Arg Ala Lys Ala Gly Cys Ala Pro Leu Met Arg Gln Tyr Gly Phe Ala 115 120 125 Trp Pro Asp Arg Met Arg Cys Asp Arg Leu Pro Glu Gln Gly Asn Pro 130 135 140 Asp Thr Leu Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala 145 150 155 160 Pro Ser Pro Pro Arg Arg Leu Pro Pro Pro Pro Pro Gly Glu Gln Pro 165 170 175 Pro Ser Gly Ser Gly His Gly Arg Pro Pro Gly Ala Arg Pro Pro His 180 185 190 Arg Gly Gly Gly Arg Gly Gly Gly Gly Gly Asp Ala Ala Ala Pro Pro 195 200 205 Ala Arg Gly Gly Gly Gly Gly Gly Lys Ala Arg Pro Pro Gly Gly Gly 210 215 220 Ala Ala Pro Cys Glu Pro Gly Cys Gln Cys Arg Ala Pro Met Val Ser 225 230 235 240 Val Ser Ser Glu Arg His Pro Leu Tyr Asn Arg Val Lys Thr Gly Gln 245 250 255 Ile Ala Asn Cys Ala Leu Pro Cys His Asn Pro Phe Phe Ser Gln Asp 260 265 270 Glu Arg Ala Phe Thr 275 74 274 PRT Mouse 74 Met Glu Trp Gly Tyr Leu Leu Glu Val Thr Ser Leu Leu Ala Ala Leu 1 5 10 15 Ala Val Leu Gln Arg Ser Ser Gly Ala Ala Ala Ala Ser Ala Lys Glu 20 25 30 Leu Ala Cys Gln Glu Ile Thr Val Pro Leu Cys Lys Gly Ile Gly Tyr 35 40 45 Asn Tyr Thr Tyr Met Pro Asn Gln Phe Asn His Asp Thr Gln Asp Glu 50 55 60 Ala Gly Leu Glu Val His Gln Phe Trp Pro Leu Val Glu Ile Gln Cys 65 70 75 80 Ser Pro Asp Leu Lys Phe Phe Leu Cys Ser Met Tyr Thr Pro Ile Cys 85 90 95 Leu Glu Asp Tyr Lys Lys Pro Leu Pro Pro Cys Arg Ser Val Cys Glu 100 105 110 Arg Ala Lys Ala Gly Cys Ala Pro Leu Met Arg Gln Tyr Gly Phe Ala 115 120 125 Trp Pro Asp Arg Met Arg Cys Asp Arg Leu Pro Glu Gln Gly Asn Pro 130 135 140 Asp Thr Leu Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala 145 150 155 160 Pro Ser Pro Pro Arg Arg Leu Pro Pro Pro Pro Pro Pro Gly Glu Gln 165 170 175 Pro Pro Ser Gly Ser Gly His Ser Arg Pro Pro Gly Ala Arg Pro Pro 180 185 190 His Arg Gly Gly Ser Ser Arg Gly Ser Gly Asp Ala Ala Ala Ala Pro 195 200 205 Pro Ser Arg Gly Gly Lys Ala Arg Pro Pro Gly Gly Gly Ala Ala Pro 210 215 220 Cys Glu Pro Gly Cys Gln Cys Arg Ala Pro Met Val Ser Val Ser Ser 225 230 235 240 Glu Arg His Pro Leu Tyr Asn Arg Val Lys Thr Gly Gln Ile Ala Asn 245 250 255 Cys Ala Leu Pro Cys His Asn Pro Phe Phe Ser Gln Asp Glu Arg Ala 260 265 270 Phe Thr 75 231 PRT Homo sapiens 75 Met Ala Val Ala Pro Leu Arg Gly Ala Leu Leu Leu Trp Gln Leu Leu 1 5 10 15 Ala Ala Gly Gly Ala Ala Leu Glu Ile Gly Arg Phe Asp Pro Glu Arg 20 25 30 Gly Arg Gly Ala Ala Pro Cys Gln Ala Val Glu Ile Pro Met Cys Arg 35 40 45 Gly Ile Gly Tyr Asn Leu Thr Arg Met Pro Asn Leu Leu Gly His Thr 50 55 60 Ser Gln Gly Glu Ala Ala Ala Glu Leu Ala Glu Phe Ala Pro Leu Val 65 70 75 80 Gln Tyr Gly Cys His Ser His Leu Arg Phe Phe Leu Cys Ser Leu Tyr 85 90 95 Ala Pro Met Cys Thr Asp Gln Val Ser Thr Pro Ile Pro Ala Cys Arg 100 105 110 Pro Met Cys Glu Gln Ala Arg Leu Arg Cys Ala Pro Ile Met Glu Gln 115 120 125 Phe Asn Phe Gly Trp Pro Asp Ser Leu Asp Cys Ala Arg Leu Pro Thr 130 135 140 Arg Asn Asp Pro His Ala Leu Cys Met Glu Ala Pro Glu Asn Ala Thr 145 150 155 160 Ala Gly Pro Ala Glu Pro His Lys Gly Leu Gly Met Leu Pro Val Ala 165 170 175 Pro Arg Pro Ala Arg Pro Pro Gly Asp Leu Gly Pro Gly Ala Gly Gly 180 185 190 Ser Gly Thr Cys Glu Asn Pro Glu Lys Phe Gln Tyr Val Glu Lys Ser 195 200 205 Arg Ser Cys Ala Pro Arg Cys Gly Pro Gly Val Glu Val Phe Trp Ser 210 215 220 Arg Arg Asp Lys Asp Phe Ala 225 230 76 232 PRT Mouse 76 Met Ala Val Pro Pro Leu Leu Arg Gly Ala Leu Leu Leu Trp Gln Leu 1 5 10 15 Leu Ala Thr Gly Gly Ala Ala Leu Glu Ile Gly Arg Phe Asp Pro Glu 20 25 30 Arg Gly Arg Gly Pro Ala Pro Cys Gln Ala Met Glu Ile Pro Met Cys 35 40 45 Arg Gly Ile Gly Tyr Asn Leu Thr Arg Met Pro Asn Leu Leu Gly His 50 55 60 Thr Ser Gln Gly Glu Ala Ala Ala Gln Leu Ala Glu Phe Ser Pro Leu 65 70 75 80 Val Gln Tyr Gly Cys His Ser His Leu Arg Phe Phe Leu Cys Ser Leu 85 90 95 Tyr Ala Pro Met Cys Thr Asp Gln Val Ser Thr Pro Ile Pro Ala Cys 100 105 110 Arg Pro Met Cys Glu Gln Ala Arg Leu Arg Cys Ala Pro Ile Met Glu 115 120 125 Gln Phe Asn Phe Gly Trp Pro Asp Ser Leu Asp Cys Ala Arg Leu Pro 130 135 140 Thr Arg Asn Asp Pro His Ala Leu Cys Met Glu Ala Pro Glu Asn Ala 145 150 155 160 Thr Ala Gly Pro Thr Glu Pro His Lys Gly Leu Gly Met Leu Pro Val 165 170 175 Ala Pro Arg Pro Ala Arg Pro Pro Gly Asp Ser Ala Pro Gly Pro Gly 180 185 190 Ser Gly Gly Thr Cys Asp Asn Pro Glu Lys Phe Gln Tyr Val Glu Lys 195 200 205 Ser Arg Ser Cys Ala Pro Arg Cys Gly Pro Gly Val Glu Val Phe Trp 210 215 220 Ser Arg Arg Asp Lys Asp Phe Ala 225 230 77 227 PRT Homo sapiens 77 Met Gln Arg Pro Gly Pro Arg Leu Trp Leu Val Leu Gln Val Met Gly 1 5 10 15 Ser Cys Ala Ala Ile Ser Ser Met Asp Met Glu Arg Pro Gly Asp Gly 20 25 30 Lys Cys Gln Pro Ile Glu Ile Pro Met Cys Lys Asp Ile Gly Tyr Asn 35 40 45 Met Thr Arg Met Pro Asn Leu Met Gly His Glu Asn Gln Arg Glu Ala 50 55 60 Ala Ile Gln Leu His Glu Phe Ala Pro Leu Val Glu Tyr Gly Cys His 65 70 75 80 Gly His Leu Arg Phe Phe Leu Cys Ser Leu Tyr Ala Pro Met Cys Thr 85 90 95 Glu Gln Val Ser Thr Pro Ile Pro Ala Cys Arg Val Met Cys Glu Gln 100 105 110 Ala Arg Leu Lys Cys Ser Pro Ile Met Glu Gln Phe Asn Phe Lys Trp 115 120 125 Pro Asp Ser Leu Asp Cys Arg Lys Leu Pro Asn Lys Asn Asp Pro Asn 130 135 140 Tyr Leu Cys Met Glu Ala Pro Asn Asn Gly Ser Asp Glu Pro Thr Arg 145 150 155 160 Gly Ser Gly Leu Phe Pro Pro Leu Phe Arg Pro Gln Arg Pro His Ser 165 170 175 Ala Gln Glu His Pro Leu Lys Asp Gly Gly Pro Gly Arg Gly Gly Cys 180 185 190 Asp Asn Pro Gly Lys Phe His His Val Glu Lys Ser Ala Ser Cys Ala 195 200 205 Pro Leu Cys Thr Pro Gly Val Asp Val Tyr Trp Ser Arg Glu Asp Lys 210 215 220 Arg Phe Ala 225 78 29 PRT Homo sapiens 78 Asp Arg Val Val Cys Asn Asp Lys Phe Ala Glu Asp Gly Ala Arg Thr 1 5 10 15 Val Ala Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu 20 25 79 29 PRT Mouse 79 Asp Arg Val Val Cys Asn Asp Lys Phe Ala Glu Asp Gly Ala Arg Thr 1 5 10 15 Val Ala Gln Gly Thr Asn Lys Glu Gly Cys Thr Ile Leu 20 25 80 29 PRT Homo sapiens 80 Glu Arg Val Val Cys Asn Glu Arg Phe Ser Glu Asp Gly Tyr Arg Thr 1 5 10 15 Val Val Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu 20 25 81 30 PRT Homo sapiens 81 Asp Arg Val Ala Cys Asn Ala Ser Ile Pro Ala Gln Tyr Lys Ala Ser 1 5 10 15 Thr Val Thr Gln Gly Ser His Asn Lys Ala Cys Thr Met Leu 20 25 30 82 30 PRT Mouse 82 Asp Arg Val Ala Cys Asn Ala Ser Ser Pro Ala Gln Tyr Lys Ala Ser 1 5 10 15 Thr Val Thr Gln Gly Ser His Asn Lys Ala Cys Thr Met Leu 20 25 30 83 29 PRT Homo sapiens 83 Arg Glu Arg Ile Ser Cys Asp Phe Glu Glu Ala Ala Glu Pro Val Leu 1 5 10 15 Ile Gln Glu Gly Leu Lys Asn Thr Gly Cys Ala Ile Ile 20 25 84 29 PRT Mouse 84 Arg Glu Arg Ile Ser Cys Asp Phe Glu Glu Ala Ala Glu Pro Val Leu 1 5 10 15 Ile Gln Glu Gly Leu Lys Asn Thr Gly Cys Ala Ile Ile 20 25 85 26 PRT Homo sapiens 85 His Ala Ser Val Ala Cys Ser Arg Glu His Asn His Ile His Tyr Glu 1 5 10 15 Thr Thr Gly Pro Ala Leu Cys Thr Ile Val 20 25 86 30 PRT Homo sapiens 86 Asp Ser Thr Ala Cys Asn Lys Ala Asp Glu Lys Leu Glu Leu Gly Asp 1 5 10 15 Thr Val Val Leu Gly Ser Gln Asn Lys Ala Cys Thr Val Leu 20 25 30 87 30 PRT Mouse 87 Asn Ser Thr Ala Cys Asn Lys Ala Asp Glu Lys Leu Glu Leu Gly Asp 1 5 10 15 Thr Val Val Leu Gly Ser Lys Asn Lys Ala Cys Ser Val Val 20 25 30 88 29 PRT Homo sapiens 88 Asp Arg Ala Val Cys Val Glu Arg Phe Ser Asp Asp Gly Tyr Arg Thr 1 5 10 15 Val Ala Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu 20 25 89 29 PRT Mouse 89 Asp Arg Ala Val Cys Val Glu Arg Phe Ser Asp Asp Gly Tyr Arg Thr 1 5 10 15 Val Ala Gln Gly Thr Lys Lys Glu Gly Cys Thr Ile Leu 20 25 90 65 PRT Homo sapiens 90 His Glu Lys Val Ala Cys Ser Gly Gly Ala Pro Gly Ala Gly Gly Ala 1 5 10 15 Gly Gly Ala Gly Gly Ala Ala Ala Gly Ala Gly Ala Ala Gly Ala Gly 20 25 30 Ala Gly Gly Pro Gly Gly Arg Gly Glu Tyr Glu Glu Leu Gly Ala Val 35 40 45 Glu Gln His Val Arg Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr Val 50 55 60 Val 65 91 66 PRT Mouse 91 His Glu Lys Val Ala Cys Ser Gly Gly Ala Pro Gly Ala Gly Gly Arg 1 5 10 15 Gly Gly Ala Gly Gly Ala Ala Ala Ala Gly Ala Gly Ala Ala Gly Arg 20 25 30 Gly Ala Ser Ser Pro Gly Ala Arg Gly Glu Tyr Glu Glu Leu Gly Ala 35 40 45 Val Glu Gln His Val Arg Tyr Glu Thr Thr Gly Pro Ala Leu Cys Thr 50 55 60 Val Val 65 92 28 PRT Homo sapiens 92 Ala Gln Ser Val Ala Cys Asp Gln Glu Ala Gly Ala Leu Tyr Val Ile 1 5 10 15 Gln Glu Gly Leu Glu Asn Thr Gly Cys Thr Leu Val 20 25 93 28 PRT Mouse 93 Ala Gln Ser Val Ala Cys Asp Gln Glu Ala Gly Ala Leu Tyr Val Ile 1 5 10 15 Gln Glu Gly Leu Glu Asn Thr Gly Cys Thr Leu Val 20 25 94 28 PRT Homo sapiens 94 Ala Glu Ser Ile Ala Cys Asp Arg Asp Ser Gly Gln Leu Tyr Val Ile 1 5 10 15 Gln Glu Gly Leu Glu Ser Thr Gly Cys Thr Leu Val 20 25 95 25 PRT Homo sapiens 95 Gly Gln Val Asp Gly Asp Val Leu Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Asn Asn Val Asp Ala Leu Arg Gly Phe 20 25 96 25 PRT Mouse 96 Gly Gln Val Asp Gly Asp Val Leu Ser Gly Val Cys Phe Leu Gly Leu 1 5 10 15 Asn Asn Val Asp Ala Leu Arg Gly Phe 20 25 97 25 PRT Homo sapiens 97 Gly Gln Ile Asp Gly Asp Leu Leu Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Asn Ser Leu Asp Pro Leu Arg Gly Phe 20 25 98 25 PRT Homo sapiens 98 Asn Lys Ile Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Tyr Asp Val Asp Ala Leu Arg Tyr Phe 20 25 99 25 PRT Mouse 99 Asn Lys Ile Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Tyr Asp Val Asp Ala Leu Arg Tyr Phe 20 25 100 25 PRT Homo sapiens 100 Arg Leu Val Asp Ala Asp Glu Leu Thr Gly Leu Cys Tyr Val Gly Asn 1 5 10 15 Gln Asn Leu Asp Ala Leu Thr Gly Phe 20 25 101 25 PRT Mouse 101 Arg Leu Val Asp Ala Asp Glu Leu Thr Gly Leu Cys Tyr Val Gly Asn 1 5 10 15 Gln Asn Leu Asp Ala Leu Thr Gly Phe 20 25 102 25 PRT Homo sapiens 102 Ser Ser Val Asp Gly Asp Pro Val Ala Gly Ile Cys Tyr Val Gly Asn 1 5 10 15 Gln Asn Leu Asn Ser Leu Arg Arg Phe 20 25 103 25 PRT Homo sapiens 103 Asn Lys Val Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Tyr Asp Leu Asp Ala Ser Arg Tyr Phe 20 25 104 25 PRT Mouse 104 Asn Lys Val Glu Gly Asp Asn Ile Ser Gly Val Cys Phe Val Gly Leu 1 5 10 15 Tyr Asp Leu Asp Ala Ser Arg Tyr Phe 20 25 105 25 PRT Homo sapiens 105 Gly Gln Val Asp Gly Asp Leu Leu Ser Gly Val Cys Tyr Val Gly Leu 1 5 10 15 Ser Ser Val Asp Ala Leu Arg Gly Phe 20 25 106 25 PRT Mouse 106 Gly Gln Val Asp Gly Asp Leu Leu Ser Gly Val Cys Tyr Val Gly Leu 1 5 10 15 Ser Ser Val Asp Ala Leu Arg Gly Phe 20 25 107 25 PRT Homo sapiens 107 Ser Ser Val Asp Gly Asp Pro Val Ala Gly Ile Cys Tyr Val Gly Asn 1 5 10 15 Gln Ser Leu Asp Asn Leu Arg Gly Phe 20 25 108 25 PRT Mouse 108 Ser Ser Val Asp Gly Asp Pro Val Ala Gly Ile Cys Tyr Val Gly Asn 1 5 10 15 Gln Ser Leu Asp Asn Leu Arg Gly Phe 20 25 109 25 PRT Homo sapiens 109 Arg Lys Val Ala Gly Asp Glu Leu Thr Gly Leu Cys Tyr Val Ala Ser 1 5 10 15 Thr Asp Ala Ala Ala Leu Thr Gly Phe 20 25 110 25 PRT Mouse 110 Arg Lys Val Ala Gly Asp Glu Leu Thr Gly Leu Cys Tyr Val Ala Ser 1 5 10 15 Met Asp Pro Ala Ala Leu Thr Gly Phe 20 25 111 24 PRT Homo sapiens 111 Arg Arg Val Ala Gly Asp Glu Leu Thr Gly Val Cys Tyr Val Gly Ser 1 5 10 15 Met Asp Val Asn Ala Leu Thr Gly 20 112 39 PRT Homo sapiens 112 Ala Phe Arg Asp Gln Trp Glu Arg Ser Trp Val Ala Gln Ser Cys Lys 1 5 10 15 Ser Tyr Ala Ile Pro Cys Pro His Leu Gln Ala Gly Gly Gly Ala Pro 20 25 30 Pro His Pro Pro Met Ser Pro 35 113 39 PRT Mouse 113 Ala Phe Arg Asp Gln Trp Glu Arg Ser Trp Val Ala Gln Ser Cys Lys 1 5 10 15 Ser Tyr Ala Ile Pro Cys Pro His Leu Gln Gly Gly Gly Gly Val Pro 20 25 30 Pro His Pro Pro Met Ser Pro 35 114 32 PRT Homo sapiens 114 Ala Phe Arg Glu His Trp Glu Arg Ser Trp Val Ser Gln His Cys Lys 1 5 10 15 Ser Leu Ala Ile Pro Cys Pro Ala His Tyr Thr Pro Arg Met Ser Pro 20 25 30 115 32 PRT Homo sapiens 115 Ala Tyr Arg Gly Ile Trp Glu Thr Thr Trp Ile Gln Glu Arg Cys Arg 1 5 10 15 Glu Tyr His Ile Pro Cys Pro Tyr Gln Val Thr Gln Met Ser Arg Pro 20 25 30 116 32 PRT Mouse 116 Ala Tyr Arg Gly Ile Trp Glu Thr Thr Trp Ile Gln Glu Arg Cys Arg 1 5 10 15 Glu Tyr His Ile Pro Cys Pro Tyr Gln Val Thr Gln Met Ser Arg Pro 20 25 30 117 17 PRT Homo sapiens 117 Ser Asn Trp Ala Leu Phe Arg Tyr Ser Ala Asp Asp Ser Asn Met Ala 1 5 10 15 Val 118 17 PRT Mouse 118 Ser Asn Trp Ala Leu Phe Arg Tyr Ser Ala Asp Asp Ser Asn Met Ala 1 5 10 15 Val 119 26 PRT Homo sapiens 119 His Tyr Arg Glu Ser Trp Glu Ala Ala Leu Thr Cys Ala Cys Pro Gly 1 5 10 15 His Asp Thr Gly Gln Pro Arg Ala Lys Pro 20 25 120 32 PRT Homo sapiens 120 Val Asn Arg Ile Thr Trp Glu Ile Thr Trp Val Ser Asp His Cys Arg 1 5 10 15 Gln Tyr His Ile Pro Cys Pro Tyr Gln Ala Lys Ala Lys Ala Arg Pro 20 25 30 121 32 PRT Mouse 121 Val Asn Arg Ile Thr Trp Glu Met Thr Trp Phe Ser Asp His Cys His 1 5 10 15 Gln Tyr Arg Ile Pro Cys Pro Tyr Gln Ala Asn Pro Lys Ala Arg Pro 20 25 30 122 32 PRT Homo sapiens 122 Ala Phe Arg Glu His Trp Glu Arg Thr Trp Leu Leu Gln Thr Cys Lys 1 5 10 15 Ser Tyr Ala Val Pro Cys Pro Pro Gly His Phe Pro Pro Met Ser Pro 20 25 30 123 32 PRT Mouse 123 Ala Phe Arg Glu His Trp Glu Arg Thr Trp Leu Leu Gln Thr Cys Lys 1 5 10 15 Ser Tyr Ala Val Pro Cys Pro Pro Arg His Phe Ser Pro Met Ser Pro 20 25 30 124 26 PRT Homo sapiens 124 His Asn Arg Pro Arg Trp Glu Ala Thr His Asn Cys Pro Cys Leu Arg 1 5 10 15 Asp Leu Gln Pro Asp Gln Ala Arg Arg Pro 20 25 125 26 PRT Mouse 125 His Asn Arg Pro Arg Trp Glu Ala Thr His Asn Cys Pro Cys Leu Arg 1 5 10 15 Asp Leu Gln Pro Asp Gln Ala Arg Arg Pro 20 25 126 35 PRT Homo sapiens 126 Leu Asn Met Asp Phe Trp Arg Leu Arg Ala Thr Glu Gln Pro Cys Ala 1 5 10 15 Ala Ala Ala Gly Pro Gly Gly Arg Arg Asp Cys Ser Leu Pro Gly Gly 20 25 30 Ser Val Pro 35 127 35 PRT Mouse 127 Leu Asn Met Asp Phe Trp Arg Leu Arg Ala Thr Glu Gln Pro Cys Thr 1 5 10 15 Ala Ala Thr Val Pro Gly Gly Arg Arg Asp Cys Ser Leu Pro Gly Gly 20 25 30 Ser Val Pro 35 128 33 PRT Homo sapiens 128 Leu Asn Met Asp Tyr Trp Lys Ile Leu Ala Ala Gln His Lys Cys Lys 1 5 10 15 Met Asn Asn Gln Thr Lys Thr Leu Asp Cys Leu Met Ala Ala Ser Ile 20 25 30 Pro 129 48 PRT Homo sapiens 129 Val Gly Gln Asn Thr Ser Asp Lys Gly Thr Pro Ser Leu Leu Pro Glu 1 5 10 15 Phe Trp Thr Ser Asn Pro Gln His Gly Gly Gly His Arg Gly Gly Phe 20 25 30 Pro Gly Gly Ala Gly Ala Ser Glu Arg Gly Lys Phe Ser Cys Pro Arg 35 40 45 130 51 PRT Homo sapiens 130 Val Gly Gln Asn His Ser Glu Asp Gly Ala Pro Ala Leu Leu Thr Thr 1 5 10 15 Ala Pro Pro Pro Gly Leu Gln Pro Gly Ala Gly Gly Thr Pro Gly Gly 20 25 30 Pro Gly Gly Gly Gly Ala Pro Pro Arg Tyr Ala Thr Leu Glu His Pro 35 40 45 Phe His Cys 50 131 26 PRT Homo sapiens 131 Leu Val Asp Leu Asn Leu Ala Gly Glu Pro Thr Glu Gly Ala Pro Val 1 5 10 15 Ala Val Gln Arg Asp Tyr Gly Phe Trp Cys 20 25 132 20 PRT Homo sapiens 132 Cys Met Glu Gly Pro Gly Asp Glu Glu Val Pro Leu Pro His Lys Thr 1 5 10 15 Pro Ile Gln Pro 20 133 46 PRT Homo sapiens 133 Cys Met Asp Tyr Asn Arg Ser Glu Ala Thr Thr Ala Pro Pro Arg Pro 1 5 10 15 Phe Pro Ala Lys Pro Thr Leu Pro Gly Pro Pro Gly Ala Pro Ala Ser 20 25 30 Gly Gly Glu Cys Pro Ala Gly Gly Pro Phe Val Cys Lys Cys 35 40 45 134 26 PRT Homo sapiens 134 Thr Phe Asp Pro His Thr Glu Phe Leu Gly Pro Gln Lys Lys Thr Glu 1 5 10 15 Gln Val Gln Arg Asp Ile Gly Phe Met Cys 20 25 135 50 PRT Homo sapiens 135 Val Gly Gln Asn Thr Ser Asp Gly Ser Gly Gly Pro Gly Gly Gly Pro 1 5 10 15 Thr Ala Tyr Pro Thr Ala Pro Tyr Leu Pro Asp Leu Pro Phe Thr Ala 20 25 30 Leu Pro Pro Gly Ala Ser Asp Gly Arg Gly Arg Pro Ala Phe Pro Phe 35 40 45 Ser Cys 50 136 86 PRT Homo sapiens 136 Cys Met Asp Tyr Asn Arg Thr Asp Leu Thr Thr Ala Ala Pro Ser Pro 1 5 10 15 Pro Arg Arg Leu Pro Pro Pro Pro Pro Gly Glu Gln Pro Pro Ser Gly 20 25 30 Ser Gly His Gly Arg Pro Pro Gly Ala Arg Pro Pro His Arg Gly Gly 35 40 45 Gly Arg Gly Gly Gly Gly Asp Ala Ala Ala Pro Pro Ala Arg Gly Gly 50 55 60 Gly Gly Gly Gly Lys Ala Arg Pro Pro Gly Gly Gly Ala Ala Pro Cys 65 70 75 80 Glu Pro Gly Cys Gln Cys 85 137 37 PRT Homo sapiens 137 Cys Met Glu Ala Pro Glu Asn Ala Thr Ala Gly Pro Ala Glu Pro His 1 5 10 15 Lys Gly Leu Gly Met Leu Pro Val Ala Pro Arg Pro Ala Arg Pro Pro 20 25 30 Gly Asp Leu Gly Pro 35 138 38 PRT Homo sapiens 138 Asn Tyr Leu Cys Val Glu Ala Pro Asn Asn Gly Ser Asp Glu Pro Thr 1 5 10 15 Arg Gly Ser Gly Leu Phe Pro Pro Leu Phe Arg Pro Gln Arg Pro His 20 25 30 Ser Ala Gln Glu His Pro 35 

We claim:
 1. A purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell.
 2. The purified antibody of claim 1, wherein the extracellular domain comprises an amino terminal peptide fragment of the frizzled receptor.
 3. The purified antibody of claim 1 further comprising an antibody fragment having an antigen binding region that specifically binds to the epitope.
 4. The purified antibody of claim 1, wherein the antibody is capable of sensitizing malignant cells expressing the frizzled receptor to a cytotoxic factor.
 5. The purified antibody of claim 1, wherein the antibody inhibits binding of a Wnt ligand to the frizzled receptor.
 6. The purified antibody of claim 1 further comprising a detectable label.
 7. The purified antibody of claim 1, wherein the antibody is a human antibody.
 8. The purified antibody of claim 1, wherein the antibody is a monoclonal antibody.
 9. The purified antibody of claim 1, wherein the antibody binds to a frizzled-2 receptor amino terminal extracellular domain.
 10. The purified antibody of claim 1, wherein the frizzled receptor amino terminal extracellular domain has a sequence that is greater than 80% homologous to an amino acid sequence selected from the group Seq. ID No.s 61, 63, 64, 66, 68, 69, 71, 73, 75 and
 77. 11. An isolated nucleic acid, comprising at least one nucleotide fragment encoding a peptide having an amino acid sequence that is greater than 80% homologous to an amino acid sequence selected from the group Seq. ID No.s 61, 63, 64, 66, 68, 69, 71, 73, 75 and
 77. 12. The isolated nucleic acid of claim 11, further comprising at least one nucleotide fragment encoding a T cell epitope .
 13. A transgenic non-human animal, comprising at least one isolated nucleic acid of claim
 11. 14. A recombinant vector, comprising at least one nucleic acid according to claim 11 functionally attached to a promoter region upstream of the nucleic acid.
 15. A host cell comprising at least one recombinant vector according to claim
 14. 16. A pharmaceutical composition comprising a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell, in a pharmaceutically acceptable carrier.
 17. A method for modulating a biological activity of a malignant cell that expresses a frizzled receptor comprising administering a pharmaceutical composition comprising a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell, in a pharmaceutically acceptable carrier.
 18. A frizzled receptor epitope conjugate comprising at least one epitope in an extracellular domain of the frizzle receptor expressed on a malignant cell and at least one epitope specific to a T cell antigen.
 19. The conjugate of claim 18, wherein the T cell antigen is also an epitope in an extracellular domain of the frizzle receptor expressed on a malignant cell
 20. The conjugate of claim 18 further comprising a linker moiety.
 21. The conjugate of claim 20, wherein the linker is GPSL.
 22. A pharmaceutical composition useful as a vaccine against malignancy for administration to a patient having a predisposition for the malignancy, comprising a purified antibody for modulating a biological activity of a malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell.
 23. A method of immunizing a subject against a malignancy comprised of malignant cells that express a frizzled receptor, said method comprising the steps of: a) identifying an antibody for modulating a biological activity of the malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell; and b) administering the antibody in a pharmaceutically acceptable carrier in an amount sufficient to inhibit the malignancy.
 24. A method of treating a subject with a malignancy comprised of malignant cells that express a frizzled receptor, said method comprising the steps of:: a) identifying an antibody for modulating a biological activity of the malignant cell that expresses a frizzled receptor, wherein said antibody specifically binds to at least one epitope in an extracellular domain of the frizzle receptor expressed on the malignant cell; and b) administering the antibody in a pharmaceutically acceptable carrier in an amount sufficient to modulate a biological activity of the malignant cell.
 25. An assay for identifying a frizzled receptor expressed by a malignant cell, wherein said frizzled receptor comprises at least one epitope in an extracellular domain, comprising the steps of: a) identifying an antibody that specifically binds to the epitope; b) exposing a sample of cells suspected of expressing the frizzled receptor to the antibody; and c) determining the extent of binding of the antibody to the cells.
 26. A screening assay for identification of small molecules that modulate frizzled receptor activity, comprising: a) selecting a library of the small molecules comprising a plurality of different chemical structures; b) contacting the small moleucles with an extracellular domain of a frizzled receptor which is capable of binding to its corresponding Wnt protein; and c) measuring binding of a ligand to the frizzled receptor in the presence of the small molecule, wherein the ligand is selected from the group consisting of the small molecule, the Wnt protein, and an antibody to the extracellular domain of the frizzled receptor. 